P3.23 Characterization of a new mutation in the GADP1 gene...

Neuromuscular Disorders 2011 Vol. 21; Iss. 9-10

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

M. Guijarro, P. Blanco-Arias, J. Pardo, C. Concheiro-Álvarez, B. San Millán, J. Joglar-Santos, M. Arias-Gómez, C. Navarro Fernández-Balbuena, A. Carracedo Álvarez, M. Sobrido
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.917
File:
PDF, 59 KB
english, 2011
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