Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

Kiyoshi Hayasaka(Akita University), Masato Himoro(Akita University), Wataru Sato(Akita University), Goro Takada(Akita University), Keiichi Uyemura(Akita University), Nobuyoshi Shimizu(Keio University), Thomas D. Bird(Akita University), P. Michael Conneally(Indiana University – Purdue University Indianapolis), Phillip F. Chance(Children's Hospital of Philadelphia)
Nature Genetics
September 1, 1993
Cited by 364

Abstract


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