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Q36077007-11A9F3D0-5A94-4FDF-B64B-6B54848F7B88
Q36077007-11A9F3D0-5A94-4FDF-B64B-6B54848F7B88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-11A9F3D0-5A94-4FDF-B64B-6B54848F7B88
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
P2860
Q36077007-11A9F3D0-5A94-4FDF-B64B-6B54848F7B88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-11A9F3D0-5A94-4FDF-B64B-6B54848F7B88
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Statement
wasDerivedFrom
0852f0a92be68ea2e19ed5b3ead39ad0dd406e3c
P2860
IQCB1 mutations in patients with leber congenital amaurosis.