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Q24647358-3CA36D18-10FF-4487-B76D-BC3069BB45D9
Q24647358-3CA36D18-10FF-4487-B76D-BC3069BB45D9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24647358-3CA36D18-10FF-4487-B76D-BC3069BB45D9
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa
P2860
Q24647358-3CA36D18-10FF-4487-B76D-BC3069BB45D9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24647358-3CA36D18-10FF-4487-B76D-BC3069BB45D9
rank
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type
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Statement
wasDerivedFrom
99099f0adf502c6980d461beb4a74c0402a67019
P2860
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor