Suggestions

Du même auteur

Novel recessive splice site mutation in POPDC1 ( BVES ) is associated with first-degree atrioventricular block and muscular dystrophy

Archive ouverte | Nelson, I. | CCSD

International audience

Genetic characterization of a French cohort of GNE -mutation negative inclusion body myopathy patients using exome sequencing

Archive ouverte | Cerino, Mathieu | CCSD

International audience

LGMD, exercise intolerance, ptosis, ophthalmoplegia and dermatologic features: the phenotypic pleiotropy of plectinopathies in 8 French families

Archive ouverte | Ben Yaou, R. | CCSD

International audience

Chargement des enrichissements...