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Q33645591-9452EB34-1F31-434C-9256-D78A3F21FA60
Q33645591-9452EB34-1F31-434C-9256-D78A3F21FA60
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-9452EB34-1F31-434C-9256-D78A3F21FA60
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype
P2860
Q33645591-9452EB34-1F31-434C-9256-D78A3F21FA60
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-9452EB34-1F31-434C-9256-D78A3F21FA60
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Statement
wasDerivedFrom
bf2fb07a106cb3a95538330f25a9e211d888f542
P2860
Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mapping.