OPA3
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- DeutschOPA3
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Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene.
Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene. ==Clinical significance== Costeff syndrome, or 3-methylglutaconic aciduria type III, is a genetic disorder caused by mutations in the OPA3 gene. In addition these mutations disrupt the production of non-shivering heat, as indicated by the dramatic decrease in surface body temperature. OMIM entries on 3-Methylglutaconic Aciduria Type 3
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