Zobrazeno 1 - 3
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pro vyhledávání: '"F, Pinto Vairo"'
Autor:
Larissa Souza Mario Bueno, M.C. Machado-Costa, M.M. Becker, Anamarli Nucci, L.S. Ferreira, M.C.S. Rodrigues, Carlo Domenico Marrone, L.V.B. Magalhães, G.N. Manzoli, Pablo Brea Winckler, Ursula da Silveira Matte, P.A.D. de Almeida, S.L. Cossio, F. Pinto Vairo, G.S. Macedo, Marina Siebert, Marília Matos Gonçalves, Jonas Alex Morales Saute, Marcondes C. França
Publikováno v:
Clinical Genetics. 92:199-203
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a7bf53caa90bf27c70c2a1ecfb983e
https://doi.org/10.1111/cge.12975
https://doi.org/10.1111/cge.12975
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26108038480160382a1a33603600f74a
https://pubmed.ncbi.nlm.nih.gov/28116794
https://pubmed.ncbi.nlm.nih.gov/28116794
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