학술논문
Congenital muscular dystrophies with defective glycosylation of dystroglycan
Document Type
Article
Author
Mercuri, E; Messina, S; Bruno, C; Mora, M; Pegoraro, E; Comi, G P.; D'Amico, A; Aiello, C; Biancheri, R; Berardinelli, A; Boffi, P; Cassandrini, D; Laverda, A; Moggio, M; Morandi, L; Moroni, I; Pane, M; Pezzani, R; Pichiecchio, A; Pini, A; Minetti, C; Mongini, T; Mottarelli, E; Ricci, E; Ruggieri, A; Saredi, S; Scuderi, C; Tessa, A; Toscano, A; Tortorella, G; Trevisan, C P.; Uggetti, C; Vasco, G; Santorelli, F M.; Bertini, E
Source
Neurology (Ovid); May 2009, Vol. 72 Issue: 21 p1802-1809, 8p
Subject
Language
ISSN
00283878; 1526632X
Abstract
Congenital muscular dystrophies (CMD) with reduced glycosylation of alpha-dystroglycan (-DG) are a heterogeneous group of conditions associated with mutations in six genes encoding proven or putative glycosyltransferases.