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Q33645591-40F8A02F-87B6-4432-A21B-C6AD1E2CF1B1
Q33645591-40F8A02F-87B6-4432-A21B-C6AD1E2CF1B1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-40F8A02F-87B6-4432-A21B-C6AD1E2CF1B1
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype
P2860
Q33645591-40F8A02F-87B6-4432-A21B-C6AD1E2CF1B1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-40F8A02F-87B6-4432-A21B-C6AD1E2CF1B1
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Statement
wasDerivedFrom
ac7223bf363eba3da26b647f22ae8f1201cfa874
P2860
Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness