论文信息 - Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis - 字舞流文

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

C. Richelme | M. Nissinen | A. Barois | K. Tryggvason | A. Helbling-Leclerc | H. Topaloglu | M. Fardeau | P. Guicheney | K. Schwartz | F. Tomé | L. Merlini | J. Lambert | N. Vignier | Xu Zhang | Corrinne Cruaud | H. Topaloğlu