Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4728
Gene Symbol: NDUFS8
NDUFS8
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2
0.600 GeneticVariation UNIPROT Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing. 22499348

2012

Entrez Id: 4728
Gene Symbol: NDUFS8
NDUFS8
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2
0.600 GeneticVariation UNIPROT Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations. 15159508

2004

Entrez Id: 4728
Gene Symbol: NDUFS8
NDUFS8
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2
0.600 GeneticVariation UNIPROT The first nuclear-encoded complex I mutation in a patient with Leigh syndrome. 9837812

1998