论文信息 - Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family - 字舞流文

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family

R. Barrantes | U. Schlötzer-Schrehardt | B. Neundörfer | B. Rautenstrauss | A. Reis | A. Leal | D. Heuss | M. Berghoff | G. del Valle | Corinna Berghoff | Carlos Contreras | Olga Montoya | E. Hernández | B. Neundörfer