Gene: NDUFA10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.300 Biomarker disease CLINGEN Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation. 28247337 2017
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.300 Biomarker disease CLINGEN Structure of mammalian respiratory complex I. 27509854 2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.300 Biomarker disease CLINGEN Accessory subunits are integral for assembly and function of human mitochondrial complex I. 27626371 2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.300 Biomarker disease CLINGEN Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9. 22200994 2012
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.300 Biomarker disease CLINGEN NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. 21150889 2011