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List of works by Valérie Allamand

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

scientific article

Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy

scientific article

Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy

scientific article

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

scientific journal article

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