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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease
Montecchiani, C., Pedace, L., Lo Giudice, T., Casella, A., Mearini, M., Gaudiello, F., Pedroso, J. L., Terracciano, C., Caltagirone, C., Massa, R., St George-Hyslop, P. H., Barsottini, O. G. P., KawarLangue:
english
Journal:
Brain
DOI:
10.1093/brain/awv320
Date:
November, 2015
Fichier:
PDF, 1.78 MB
english, 2015