Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
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D. Bonneau | P. Amati‐Bonneau | P. Reynier | V. Procaccio | L. Richard | F. Dubas | C. Verny | M. Ferré | A. Chevrollier | N. Gueguen | J. Cassereau | G. Nicolas | F. Letournel | M. Malinge