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Q33693684-87B7480D-B273-4DF9-8872-9D65FA211B6B
Q33693684-87B7480D-B273-4DF9-8872-9D65FA211B6B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33693684-87B7480D-B273-4DF9-8872-9D65FA211B6B
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.
P2860
Q33693684-87B7480D-B273-4DF9-8872-9D65FA211B6B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33693684-87B7480D-B273-4DF9-8872-9D65FA211B6B
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type
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wasDerivedFrom
6d0246ac0e58ff80f76abf67a040a84448877ddc
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