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Q35944038-6F9501BE-C8B1-4886-8881-3DE343C10D08
Q35944038-6F9501BE-C8B1-4886-8881-3DE343C10D08
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http://www.wikidata.org/entity/statement/Q35944038-6F9501BE-C8B1-4886-8881-3DE343C10D08
Molecular genetic basis of primary inherited optic neuropathies.
P2860
Q35944038-6F9501BE-C8B1-4886-8881-3DE343C10D08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35944038-6F9501BE-C8B1-4886-8881-3DE343C10D08
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wasDerivedFrom
b9734359acbcd47a43c6058267bc99a1c68b25e0
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