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Autor:
P A D, de Almeida, M C, Machado-Costa, G N, Manzoli, L S, Ferreira, M C S, Rodrigues, L S M, Bueno, J A M, Saute, F, Pinto Vairo, U S, Matte, M, Siebert, S L, Cossio, G S, Macedo, P B, Winckler, M M, Becker, L V B, Magalhães, M V M, Gonçalves, C D, Marrone, A, Nucci, M C, França
Publikováno v:
Clinical genetics. 92(2)
Different types of mutations in the DMD gene underlie Duchenne muscular dystrophies (DMD) and Becker muscular dystrophies (BMD). Large deletions and duplications are the most frequent causative genetic alterations worldwide, but little is known about