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mitochondrial complex iii deficiency
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BCS1L
Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome
UQCRB
Mitochondrial UQCRB regulates VEGFR2 signaling in endothelial cells
Common protein-binding sites in the 5'-flanking regions of human genes for cytochrome c1 and ubiquinone-binding protein
UQCRC2
Complementary DNA encoding core protein II of human mitochondrial cytochrome bc1 complex. Substantial diversity in deduced primary structure from its yeast counterpart
CYC1
Integration of cardiac proteome biology and medicine by a specialized knowledgebase
Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia
Role of HIV Vpr as a regulator of apoptosis and an effector on bystander cells
Cancer Gene Census
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Definition
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