Suggestions

Du même auteur

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

Archive ouverte | Bitoun, Marc | CCSD

International audience

Mutations in dynamin 2 cause dominant Centronuclear Myopathy

Archive ouverte | Bitoun, Marc | CCSD

International audience. Autosomal dominant centronuclear myopathy is a rare congenital myopathy characterized by delayed motor milestones and muscular weakness. In 11 families affected by centronuclear myopathy, we ...

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

Archive ouverte | Durieux, Anne-Cécile | CCSD

International audience

Chargement des enrichissements...