论文信息 - Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study - 字舞流文

Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study

K. North | M. Chevallay | P. Guicheney | F. Tomé | N. Vignier | K. Jones | T. Mizuta | H. Hori | G. Morgan | Y. He | K. Jones | A. Barois | B. Estournet‐Mathiaud