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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 – topic of research
by: St. John A. Clottey Royal Veterinary & Agricultural University, Copenhagen, Denmark Three general classes of pathologica
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TREAT-NMD workshop: Pattern recognition in genetic muscle diseases using muscle MRI: 25–26 February 2011, Rome, Italy | Semantic Scholar
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