Condition: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6


rs121434427 in NDUFS2 gene and MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6 PMID 11220739 2001 Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy.

rs121434429 in NDUFS2;FCER1G gene and MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6 PMID 11220739 2001 Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy.