P5.20 Limb Girdle Congenital Myasthenia Syndrome associated with mutations in GFPT1 gene. Report of two patients

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2011-10, Vol.21 (9), p.729-730
Main Authors: Colomer, J, Nascimento, A, Ortez, C, Jimenez-Mallabrera, C, Jou, C, Corbera, J, Guergueltcheva, V, Senderek, J, Müller, J.S, Lochmüller, H
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.2011.06.1049