G.P.2.02 Genotype–phenotype correlations in congenital muscular dystrophies with defective glycosylation of dystroglycan: A multicentric Italian study

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2008-10, Vol.18 (9), p.735-735
Main Authors: Messina, S.M, Santorelli, F.M.S, Mora, M.M, Bruno, C.B, Pegoraro, E.P, Pini, A.P, Mongini, T.M, d’Amico, A.D, Pane, M.P, Biancheri, R.B, Berardinelli, A.B, Toscano, A.T, Morandi, L.M, Moroni, M.I, Comi, G.P.C, Uggetti, C, Trevisan, c.P.T, Farina, L.F, Pichiecchio, A.P, Scuderi, C.S, Ruggieri, A.R, Bertini, E.B, Mercuri, E.M
Format: Article
Language:English
Subjects:
Neurology
Online Access:Get full text
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ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2008.06.042