ArticleNeuromuscular disorders : NMD2012

Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.

Giulia Ricci et al.PubMed ↗Full text ↗Publisher ↗

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