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Q30440790-AC3393B1-0C8D-4188-B575-6D1FA3F7F6CC
Q30440790-AC3393B1-0C8D-4188-B575-6D1FA3F7F6CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30440790-AC3393B1-0C8D-4188-B575-6D1FA3F7F6CC
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families
P2860
Q30440790-AC3393B1-0C8D-4188-B575-6D1FA3F7F6CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30440790-AC3393B1-0C8D-4188-B575-6D1FA3F7F6CC
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wasDerivedFrom
5a5ae1233d5f38d7bdb0b125cfe24dcaf7190c40
P2860
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor