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

✍ Scribed by 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

Book ID: 116795099
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 59 KB
Volume: 21
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2011.06.917

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