(Q59697745)
Statements
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT (English)
J Cassereau
N Gueguen
M-C Malinge
V Guillet
P Amati-Bonneau
I Banchs
V Volpini
scientific article published on 01 April 2011
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