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Q36077007-17C2EA2D-2EC4-43E3-9C0D-084E8F8BFE04
Q36077007-17C2EA2D-2EC4-43E3-9C0D-084E8F8BFE04
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Statement
http://www.wikidata.org/entity/statement/Q36077007-17C2EA2D-2EC4-43E3-9C0D-084E8F8BFE04
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
P2860
Q36077007-17C2EA2D-2EC4-43E3-9C0D-084E8F8BFE04
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-17C2EA2D-2EC4-43E3-9C0D-084E8F8BFE04
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wasDerivedFrom
7b31926caf07c46e579dcdc8f379a7c7ac9a8467
P2860
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.