论文信息 - Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. - 字舞流文

Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy.

C. Walsh | Ryan N. Doan | J. Partlow | T. Ben-Omran | Nada Alaaraj | M. Almureikhi | M. Elsaid | A. James Barkovich | Shenela Lakhani | Muna Al Saffar