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Q24647358-1678D502-D5D4-4FEB-AC64-81412C81CB34
Q24647358-1678D502-D5D4-4FEB-AC64-81412C81CB34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24647358-1678D502-D5D4-4FEB-AC64-81412C81CB34
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa
P2860
Q24647358-1678D502-D5D4-4FEB-AC64-81412C81CB34
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24647358-1678D502-D5D4-4FEB-AC64-81412C81CB34
rank
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type
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Statement
wasDerivedFrom
99099f0adf502c6980d461beb4a74c0402a67019
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis