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Q33645591-7F3237F0-2D2E-4BBE-952F-91F5DDFA96CC
Q33645591-7F3237F0-2D2E-4BBE-952F-91F5DDFA96CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-7F3237F0-2D2E-4BBE-952F-91F5DDFA96CC
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype
P921
Q33645591-7F3237F0-2D2E-4BBE-952F-91F5DDFA96CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-7F3237F0-2D2E-4BBE-952F-91F5DDFA96CC
rank
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type
BestRank
Statement
P921
birth defect