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Q36989961-CA468B04-2F3B-4B8F-B1A9-74B69DC6CF71
Q36989961-CA468B04-2F3B-4B8F-B1A9-74B69DC6CF71
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http://www.wikidata.org/entity/statement/Q36989961-CA468B04-2F3B-4B8F-B1A9-74B69DC6CF71
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases
P2860
Q36989961-CA468B04-2F3B-4B8F-B1A9-74B69DC6CF71
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36989961-CA468B04-2F3B-4B8F-B1A9-74B69DC6CF71
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Statement
wasDerivedFrom
6cf5fedad3a573ae632fb67277c1c7ad390393d3
P2860
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa