P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

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Bibliographic Details
Published in:Neuromuscular disorders : NMD Vol. 21; no. 9; pp. 688 - 689
Main Authors: Guijarro, M, Blanco-Arias, P, Pardo, J, Concheiro-Álvarez, C, San Millán, B, Joglar-Santos, J, Arias-Gómez, M, Navarro Fernández-Balbuena, C, Carracedo Álvarez, A, Sobrido, M
Format: Journal Article
Language:English
Published: Elsevier B.V 01-10-2011
Subjects:
Neurology
Online Access:Get full text
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Description
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2011.06.917