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Q26770321-F3A53722-5053-482E-B294-351CEC94AFC1
Q26770321-F3A53722-5053-482E-B294-351CEC94AFC1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770321-F3A53722-5053-482E-B294-351CEC94AFC1
Retinal dystrophies, genomic applications in diagnosis and prospects for therapy
P2860
Q26770321-F3A53722-5053-482E-B294-351CEC94AFC1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770321-F3A53722-5053-482E-B294-351CEC94AFC1
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wasDerivedFrom
8a8feaf944fcbf12ad993792f4e65a52f8d4a358
P2860
A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype