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Q30494546-7089B52B-575B-4CFD-9825-DE943BFBA0E2
Q30494546-7089B52B-575B-4CFD-9825-DE943BFBA0E2
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Statement
http://www.wikidata.org/entity/statement/Q30494546-7089B52B-575B-4CFD-9825-DE943BFBA0E2
OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria
P2860
Q30494546-7089B52B-575B-4CFD-9825-DE943BFBA0E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30494546-7089B52B-575B-4CFD-9825-DE943BFBA0E2
rank
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wasDerivedFrom
03121f2b59c128d2f9b7c2034796d70d9ea6c419
P2860
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews