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This page is a summary of: 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, Neuromuscular Disorders, June 2012, Elsevier,
DOI: 10.1016/j.nmd.2011.12.001.
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