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All mouse models of combined oxidative phosphorylation deficiency with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
 | combined oxidative phosphorylation deficiency | Mto1Gt(G019A03)Wrst/Mto1Gt(G019A03)Wrst | involves: 129S2/SvPas * C57BL/6J | J:223246 | View | |||