Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
0.730 GeneticVariation UNIPROT Here, we characterize four patients with isolated complex II deficiency caused by mutations in SDHA presenting with multisystem mitochondrial disease including Leigh syndrome (LS) and/or leukodystrophy. 24781757

2015

Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
0.730 GeneticVariation UNIPROT Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. 10746566

2000

Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
0.730 GeneticVariation UNIPROT Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. 7550341

1995