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

Isabella Scionti, Greta Alì, Leda Volpi, Virna Zampa, Marina Fanin, Corrado Angelini, Luisa Politano, Rossella Tupler, Gabriele Siciliano
  • Neuromuscular Disorders, June 2012, Elsevier
  • DOI: 10.1016/j.nmd.2011.12.001

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The following have contributed to this page: Prof Corrado Angelini