O.3 Satellite cell loss is the pathomechanism leading to muscle atrophy in selenoprotein N deficiency

Archive ouverte | Castets, P. | CCSD

International audience

A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

Archive ouverte | Allamand, V. | CCSD

Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon

Archive ouverte | Rederstorff, M. | CCSD

International audience