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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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X-linked myopathy with excessive autophagy: a clinicopathological study of five new families

B Chabrol1, D Figarella-Branger, M Coquet

  • 1Department of Neuropediatrics, Hôpital Timone, Jean Moulin Boulevard, Marseille, France.

Neuromuscular Disorders : NMD
|May 23, 2001
PubMed

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