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.