WATANABE Yoriko 渡邊順子

… Alternative Names

渡邊順子ワタナベヨリコ

渡辺順子ワタナベヨリコ

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Researcher Number	40258489
Other IDs
External Links
Affiliation (Current)	2025: 久留米大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2005 – 2007: Kurume University School of Medicine, Department of Pediatrics & Child Health, Lecturer, 医学部, 講師 2002 – 2004: Department of Pediatrics and Child Health, Kurume University School of Medicine Research Associate, 医学部, 助手 1997 – 1998: 久留米大学, 医学部, 助手 1994: 久留米大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics Except Principal Investigator Pediatrics / Pediatrics
Keywords	Principal Investigator MALDI-TOF-MS / Wilson disease / hypoceruloplasminemia / proteome analysis / Cerulonlasmin / 質量分析 / ウィルソン病 / 低セルロプラスミン血症 / ペプチド解析 / セルロプラスミン … More / 内臓錯位 / 刺激伝導障害 / 家族性心房中隔欠損症 / 連鎖解析 / 刺激伝導系障害 / 心房中隔欠損症 / YAC / STS / SCID / 8q11-q13 / HYRC gene / BOR … More Except Principal Investigator screening / 発症予防 / スクリーニング / オルニチントランスカルバミラーゼ欠損症 / RNA 19 / MELAS / male patients / late-onset presentation / ornithine transcarbamylase deficiency / オルチニントランスカルバミラーゼ欠損症 / 予後因子 / 遺伝疫学 / 遅発男子例 / prevention / orinithine transcarbamylase / オルニチントランスカルパミラーゼ / 一塩基置換 / オルニチントランスカルバミラーゼ / respiratory chain enzymes / point mutation / tissue specificity / processing / mitochondrial RNA / mitochondrial DNA / 母性遺伝 / RNAプロセッシング / ミトコンドリアtRNA / ミトコンドリア脳筋症 / ミトコンドリア DNA / 電子伝達系酵素 / 点変異 / 臓器特異性 / RNA19 / プロセッシング / ミトコンドリアRNA / ミトコンドリアDNA Less

Structural Analysis of Serum Ceruloplasmin Peptides From The Patients With Wilson disease and Familial HypoccerulosminemiaPrincipal Investigator
- Principal Investigator
  
  WATANABE Yoriko
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kurume University
A study on Presymptomatic recognition and prevention of late-onset ornithine transcarbamylase deficiency in male
- Principal Investigator
  
  YOSHINO Makoto
- Project Period (FY)
  2003 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kurume University
A Study on Molecular Epidemiology and Prevention of Onset of Late-onset Ornithine Transcarbamylase Deficiency in Male Patients
- Principal Investigator
  
  YOSHINO Makoto
- Project Period (FY)
  2000 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  KURUME UNIVERSITY
先天性心疾患発症におけるNeurotrophin-3の発現Principal Investigator
- Principal Investigator
  
  渡辺順子
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Kurume University
MOLECULAR BASIS OF MITOCHONDRIAL RNA PROCESSING SYSTEM IN DEVELOPMENTAL TISSUES AND IN MITOCHONDRIAL MYOPATHY.
- Principal Investigator
  
  KOGA Yasutoshi
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  KURUME UNIVERSITY SCHOOL OF MEDICINE
鰓、耳、腎症候群(BOR)座領域のDNA多型マーカーの作製と連鎖解析Principal Investigator
- Principal Investigator
  
  渡辺順子
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Kurume University

All 2008 2007 2006 2005 2003 Other

All Journal Article Book

[Book] 小児救急学習用テキスト原著第4版2006
- Author(s)
  渡辺順子
- Total Pages
  759
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Paternal transmission and slow elimination of mutant allelesassociated with late-onset ornithine transcarbamylase deficiencyin male patients2008
- Author(s)
  Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Ybshino M
- Journal Title
  
  J Hum Genet 53
  
  Pages: 10-17
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients2008
- Author(s)
  Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Yoshino M
- Journal Title
  
  J Hum Genet 53
  
  Pages: 10-17
- NAID
  10021247384
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.2008
- Author(s)
  Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Yoshino M.
- Journal Title
  
  J Hum Genet 53(doi ; 10.1007/s10038-007-0212-8)
  
  Pages: 10-17
- NAID
  10021247384
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography.2007
- Author(s)
  Samejima H,'Ibrii C, Kosaki R, Kurosawa K, Yoshihashi H,Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi'F, Kosaki K.
- Journal Title
  
  Genet Test 11(doi : 10.1089/gte.2006.0519)
  
  Pages: 216-227
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Roles of some cytokines in bone remodeling and hematopoiesis in Gaucher disease.2007
- Author(s)
  Yoshino M, Watanabe Y, Thkunaga Y, Harada E, Fujii C, Numata S, Harada M, Tajima A, Ida H.
- Journal Title
  
  Pediatr Int 49(doi : 10.1111/j.1442-200x.2007.02502.x)
  
  Pages: 959-956
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency2007
- Author(s)
  Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T
- Journal Title
  
  J Hum Genet 52
  
  Pages: 1040-1043
- NAID
  10020022418
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoAcarboxylase deficiency2007
- Author(s)
  Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchja S, Ohura T
- Journal Title
  
  J Hum Genet 52
  
  Pages: 1040-1043
- NAID
  10020022418
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Screening for Alagille syndrome mutations in the JAGl andNOTCH2 genes using denaturing high-performance liquidchromatography2007
- Author(s)
  Samejima H, Torii C, Kosaki R, Kurosawa K, Yoshihashi H, Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi T, Kosaki K
- Journal Title
  
  Genet Test 11
  
  Pages: 216-227
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography2007
- Author(s)
  Samejima H, Torii C, Kosaki R, Kurosawa K, Yoshihashi H, Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi T, Kosaki K
- Journal Title
  
  Genet Test 11
  
  Pages: 216-227
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Roles of specific cytokines in bone remodeling and hematopoiesis in Gaucher disease2007
- Author(s)
  Yoshino M, Watanabe Y, Tokunaga Y, Harada E, Fujii C, Numata S, Harada M, Tajima A, Ida H
- Journal Title
  
  Pediatr Int 49
  
  Pages: 959-965
- NAID
  10024152088
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-C0A carboxylase deficiency.2007
- Author(s)
  Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T,Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M,Watanabe Y, Inokuchi T, Yokoyama T. Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T.
- Journal Title
  
  J Hum Genet. 52(doi : 10.1007/s10038-007-0211-9)
  
  Pages: 1040-1043
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] 栄養療法で急性期治療を行ったメープルシロップ尿症の1例2006
- Author(s)
  岡田純一郎, 渡辺順子, 平井裕子, 神戸太郎, 廣瀬彰子, 藤野浩, 前野泰樹, 芳野信
- Journal Title
  
  日本マススクリーニング学会雑誌 16
  
  Pages: 63-67
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M.
- Journal Title
  
  Pediatr Int 48
  
  Pages: 105-111
- NAID
  10018195131
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients:Prognostic factors and characteristics of plasma amino acid profile2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
- Journal Title
  
  Pediatr Int 48
  
  Pages: 105-111
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes2006
- Author(s)
  Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N
- Journal Title
  
  Am J Med Genet A 140・16
  
  Pages: 1719-1725
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Late-onset Ornithine Transcarbamylase Deficiency in Male Patients : Prognostic Factors and Characteristics of Plasma Amino Acid Profile2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
- Journal Title
  
  Pediatrics International 48
  
  Pages: 105-111
- NAID
  10018195131
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Late-onset ornithine transcarbamylase deficiency inmale patients:Prognostic factors and characteristics of plasma amino acid profile.2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N,Kumasbiro R, Kuno T, Kuromaru R, Hirose 5, Ichikawa K,Yoshino M.
- Journal Title
  
  Pediatr Int 48(doi : 10.1111/j.1442-200x.02181.x)
  
  Pages: 105-111
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.2006
- Author(s)
  Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N
- Journal Title
  
  Am J Med Genet A 140・16
  
  Pages: 1719-1725
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Comprehensive genetic analysis of relevant fourgenes in 49 patients with Marfan syndrome or Marfan-related phenotypes.2006
- Author(s)
  Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N,Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N.
- Journal Title
  
  Am J Med GenetA. 140(16)(doi : 10.1002/ajmg.a.31353)
  
  Pages: 1719-25
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
- Journal Title
  
  Pediatr Int 48
  
  Pages: 105-111
- NAID
  10018195131
- Data Source
  KAKENHI-PROJECT-17591125
[Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006
- Author(s)
  Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
- Journal Title
  
  Pediatr Int 48
  
  Pages: 105-111
- NAID
  10018195131
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Ornithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability2005
- Author(s)
  Watanabe Y, Harada E, Yoshino M
- Journal Title
  
  Journal of Inherited Metabolic Disease 28・suppl.
  
  Pages: 67-67
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] 男子OTC欠損症:新生児例と遅発例の変異の対比2005
- Author(s)
  首藤紳介, 渡辺順子, 原田英明, 西依淳, 前野泰樹, 竹中聡, 井上敏郎, 井上真改, 合志光史
- Journal Title
  
  日本先天代謝異常学会雑誌 21
  
  Pages: 74-74
- NAID
  10016759792
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Ornithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability2005
- Author(s)
  Watanabe Y, Harada H, Yoshino M
- Journal Title
  
  J Inherit Metab Dis 28 - suppl.
  
  Pages: 67-67
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Omithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability.2005
- Author(s)
  Watanabe Y, Harada H, Yoshino M.
- Journal Title
  
  J Inherit Metab Dis 28 suppl
  
  Pages: 67-67
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] 男子OTC欠損症 : 新生児例と遅発例の変異の対比2005
- Author(s)
  首藤紳介, 渡辺順子, 原田英明, 西依淳, 前野泰樹, 竹中聡, 井上敏郎, 井上真改, 合志光史
- Journal Title
  
  日本先天代謝異常学会雑誌 21
  
  Pages: 74-74
- NAID
  10016759792
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Effect of supplementation with L-carnitine at a small dose on acycarnitine profiles in serum and urine andthe renal handling of acylcarnitines in a patient withmultiple acylcoenzyme A dehydrogenation defect.2003
- Author(s)
  Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S.
- Journal Title
  
  J Chromatogr B 792
  
  Pages: 73-82
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] Effect of supplementation with L-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect.2003
- Author(s)
  Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S
- Journal Title
  
  J Chromatogr B 792
  
  Pages: 73-82
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591148
[Journal Article] OTC deficiency in male : a comparison of mutations in the neonatal onset with those in the late-onset presentations.
- Author(s)
  Shuto S, Watanabe Y, Harada E, Nishiyori A, Maeno Y, Takenaka S, Inoue T, Inoue S, Goshi T.
- Journal Title
  
  J Jpn Soc Inher Metab Dis 21
  
  Pages: 74-74
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591148

1. YOSHINO Makoto (40080569)

# of Collaborated Projects: 3 results

# of Collaborated Products: 19 results
2. HARADA Eimei (90309790)

# of Collaborated Projects: 3 results

# of Collaborated Products: 20 results
3. KOGA Yasutoshi (00225400)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. YANO Shoji (00220202)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 徳永泰幸 (60227585)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

WATANABE Yoriko 渡邊 順子

渡邊 順子 ワタナベ ヨリコ

渡辺 順子 ワタナベ ヨリコ

Research Projects

Research Products

Co-Researchers

Structural Analysis of Serum Ceruloplasmin Peptides From The Patients With Wilson disease and Familial HypoccerulosminemiaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

A study on Presymptomatic recognition and prevention of late-onset ornithine transcarbamylase deficiency in male

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

A Study on Molecular Epidemiology and Prevention of Onset of Late-onset Ornithine Transcarbamylase Deficiency in Male Patients

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

先天性心疾患発症におけるNeurotrophin-3の発現Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

MOLECULAR BASIS OF MITOCHONDRIAL RNA PROCESSING SYSTEM IN DEVELOPMENTAL TISSUES AND IN MITOCHONDRIAL MYOPATHY.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

鰓、耳、腎症候群(BOR)座領域のDNA多型マーカーの作製と連鎖解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 小児救急学習用テキスト原著第4版2006

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] Paternal transmission and slow elimination of mutant allelesassociated with late-onset ornithine transcarbamylase deficiencyin male patients2008

Author(s)

Journal Title

Data Source

[Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients2008

Author(s)

Journal Title

NAID

Description

Data Source

[Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.2008

Author(s)

Journal Title

NAID

Description

Data Source

[Journal Article] Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography.2007

Author(s)

Journal Title

Description

Data Source

[Journal Article] Roles of some cytokines in bone remodeling and hematopoiesis in Gaucher disease.2007

Author(s)

Journal Title

Description

Data Source

[Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency2007

Author(s)

Journal Title

NAID

Description

Data Source

[Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoAcarboxylase deficiency2007

WATANABE Yoriko 渡邊順子

渡邊順子ワタナベヨリコ

渡辺順子ワタナベヨリコ