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
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| Description | scientific article |
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author: Corrado Angelini Greta Alì Rossella Tupler Giulia Ricci Gabriele Siciliano |
| Publication date | January 14, 2012 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |