Gene: NDUFS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4720
Gene Symbol: NDUFS2
NDUFS2 		0.320 Biomarker group CTD_human While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy. 14729820 2004
Entrez Id: 4720
Gene Symbol: NDUFS2
NDUFS2 		0.320 GeneticVariation group BEFREE While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy. 14729820 2004
Entrez Id: 4720
Gene Symbol: NDUFS2
NDUFS2 		0.320 GeneticVariation group BEFREE Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy. 11220739 2001