Gene: SDHA ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors. 24781757 2015
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. 22972948 2012
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy. 19465911 2009
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex II. 16798039 2006
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN 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 		0.300 Biomarker disease CLINGEN Suppression of sdh1 mutations by the SDH1b gene of Saccharomyces cerevisiae. 9730279 1998
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. 7550341 1995
Entrez Id: 6389
Gene Symbol: SDHA
SDHA 		0.300 Biomarker disease CLINGEN SDH1, the gene encoding the succinate dehydrogenase flavoprotein subunit from Saccharomyces cerevisiae. 1511876 1992