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Q24291826-01C2CC47-6E89-4FC2-B0DE-FB4EF0170B0A
Q24291826-01C2CC47-6E89-4FC2-B0DE-FB4EF0170B0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24291826-01C2CC47-6E89-4FC2-B0DE-FB4EF0170B0A
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
P2860
Q24291826-01C2CC47-6E89-4FC2-B0DE-FB4EF0170B0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24291826-01C2CC47-6E89-4FC2-B0DE-FB4EF0170B0A
rank
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type
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Statement
wasDerivedFrom
7453fa95b9748838ff72cc7012eccbeefbee8e56
P2860
A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia.