Gene: ND3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4537
Gene Symbol: ND3
ND3 		0.030 GeneticVariation disease BEFREE The present case confirms that the clinical spectrum of Complex I deficiency related to T10158C mutation ND3 gene is wider than previously described. 27742419 2017
Entrez Id: 4537
Gene Symbol: ND3
ND3 		0.030 GeneticVariation disease BEFREE A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia. 17152068 2007
Entrez Id: 4537
Gene Symbol: ND3
ND3 		0.030 GeneticVariation disease BEFREE De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. 14705112 2004