Publication | Closed Access
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
84
Citations
14
References
2008
Year
Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsPathogenesisPathologyMitochondrial MedicineMolecular GeneticsDisease Gene IdentificationMitochondrial ComplexMedicine
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