Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients: two familial and three sporadic cases including the first Japanese patient with medulloblastoma
Bibliographic Information
- Other Title
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- Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients two familial and three sporadic cases including the first Japanese patient with medulloblastoma
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Journal
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- Journal of human genetics / Japan Society of Human Genetics
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Journal of human genetics / Japan Society of Human Genetics 56 (4), 277-283, 2011-04
Tokyo : Springer Nature
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Keywords
Details
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- CRID
- 1521699230209530624
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- NII Article ID
- 40018765626
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- NII Book ID
- AA11206160
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- ISSN
- 14345161
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- NDL BIB ID
- 11045788
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- Text Lang
- en
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- NDL Source Classification
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- ZS16(科学技術--医学--人類遺伝学)
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- Data Source
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- NDL
- CiNii Articles