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Q36901097-1699F9F3-A986-4F49-81F1-CC092975AF33
Q36901097-1699F9F3-A986-4F49-81F1-CC092975AF33
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http://www.wikidata.org/entity/statement/Q36901097-1699F9F3-A986-4F49-81F1-CC092975AF33
Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa.
P2860
Q36901097-1699F9F3-A986-4F49-81F1-CC092975AF33
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36901097-1699F9F3-A986-4F49-81F1-CC092975AF33
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wasDerivedFrom
cf015d2c252cbe1767aed599cf9776cbf06ba65f
P2860
Exome Sequencing Identified a Recessive RDH12 Mutation in a Family with Severe Early-Onset Retinitis Pigmentosa.