Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT
Cassereau, J., Casasnovas, C., Gueguen, N., Malinge, M.- C., Guillet, V., Reynier, P., Bonneau, D., Amati-Bonneau, P., Banchs, I., Volpini, V., Procaccio, V., Chevrollier, A.Volume:
76
Langue:
english
Journal:
Neurology
DOI:
10.1212/WNL.0b013e318217e77d
Date:
April, 2011
Fichier:
PDF, 620 KB
english, 2011