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 		0.510 Biomarker disease CLINGEN Here, we present an additional description of a child with Leigh syndrome harboring a homozygous mutation in NDUFA10, providing insights in clinical, biochemical, and neuroradiologic features for future earlier recognition. 28247337 2017
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 Biomarker disease GENOMICS_ENGLAND Here, we present an additional description of a child with Leigh syndrome harboring a homozygous mutation in NDUFA10, providing insights in clinical, biochemical, and neuroradiologic features for future earlier recognition. 28247337 2017
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 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 		0.510 Biomarker disease GENOMICS_ENGLAND A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies. 26741492 2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 Biomarker disease CLINGEN Structure of mammalian respiratory complex I. 27509854 2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 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 		0.510 Biomarker disease GENOMICS_ENGLAND NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. 21150889 2011
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 GeneticVariation disease BEFREE NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. 21150889 2011
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 Biomarker disease CLINGEN NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. 21150889 2011
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10 		0.510 Biomarker disease GENOMICS_ENGLAND