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Q36077007-1EA7EF76-6D04-43FB-B71F-9F7602F5D9D0
Q36077007-1EA7EF76-6D04-43FB-B71F-9F7602F5D9D0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-1EA7EF76-6D04-43FB-B71F-9F7602F5D9D0
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
P2860
Q36077007-1EA7EF76-6D04-43FB-B71F-9F7602F5D9D0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-1EA7EF76-6D04-43FB-B71F-9F7602F5D9D0
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wasDerivedFrom
0852f0a92be68ea2e19ed5b3ead39ad0dd406e3c
P2860
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.