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
  • Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients two familial and three sporadic cases including the first Japanese patient with medulloblastoma

Search this article

Journal

Details

Report a problem

Back to top