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 adouble troublea overlapping syndromes
Ricci, Giulia, Scionti, Isabella, AlAn, Greta, Volpi, Leda, Zampa, Virna, Fanin, Marina, Angelini, Corrado, Politano, Luisa, Tupler, Rossella, Siciliano, Gabriele
Published in Neuromuscular disorders : NMD (01.06.2012)
Published in Neuromuscular disorders : NMD (01.06.2012)
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