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Q33645591-079498F5-F19F-48E9-8140-B9E1CC00D19B
Q33645591-079498F5-F19F-48E9-8140-B9E1CC00D19B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-079498F5-F19F-48E9-8140-B9E1CC00D19B
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype
P2860
Q33645591-079498F5-F19F-48E9-8140-B9E1CC00D19B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33645591-079498F5-F19F-48E9-8140-B9E1CC00D19B
rank
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Statement
wasDerivedFrom
bf2fb07a106cb3a95538330f25a9e211d888f542
P2860
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.