Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Leoberto R, Grigollo"'
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a45cf40d1bbd8071aa23ee79214db7
Autor:
Clarissa M, Comim, Jaime A, Soares, Adriano, Alberti, Viviane, Freiberger, Letícia, Ventura, Paula, Dias, Aryadnne L, Schactae, Leoberto R, Grigollo, Amanda V, Steckert, Daniel F, Martins, Rudy J Nodari, Junior, Mariz, Vainzof, João, Quevedo
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyReferences. 43(7)
Congenital Muscular Dystrophy type 1D (MDC1D) is characterized by a hypoglycosylation of α-dystroglycan protein (α-DG), and this may be strongly implicated in increased skeletal muscle tissue degeneration and abnormal brain development, leading to