(Q38917391)
Statements
Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C (English)
Bernd Wollnik
Abdelhamid Barakat
Omar Abidi
Redouane Boulouiz
Abdelaziz Chafik
Yun Li
Hanno Bolz
Hassan Roub
Christian Kubisch