A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation
Titel:
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation
Auteur:
Neri, M. Selvatici, R. Scotton, C. Trabanelli, C. Armaroli, A. De Grandis, D. Levy, N. Gualandi, F. Ferlini, A.