OBO ID: DOID:0111143 |
Term Name: | mitochondrial complex V (ATP synthase) deficiency | Search Ontology: | |
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Definition: | A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex. https://www.ncbi.nlm.nih.gov/pubmed/21874297 | ||
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Ontology: | Human Disease ( DOID:0111143 ) |
OTHER mitochondrial complex V (ATP synthase) deficiency PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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