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Q38725572-153E789E-3130-4735-AA68-9EA27680580A
Q38725572-153E789E-3130-4735-AA68-9EA27680580A
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Statement
http://www.wikidata.org/entity/statement/Q38725572-153E789E-3130-4735-AA68-9EA27680580A
Variant haploinsufficiency and phenotypic non-penetrance in PRPF31-associated retinitis pigmentosa.
P2860
Q38725572-153E789E-3130-4735-AA68-9EA27680580A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38725572-153E789E-3130-4735-AA68-9EA27680580A
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wasDerivedFrom
06940ba6518736bfbcacee9de40ed2124e6b5df1
P2860
Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa.