| 1 | RP1L1, RP88
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| Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients
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| Albarry MA, Hashmi JA, Alreheli AQ, Albalawi AM, Khan B, Ramzan K, Basit S.
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| Ophthalmic Genet. Dec;40(6):507-513. doi: 10.1080/13816810.2019.1703014. Epub 2019 Dec 13. 2019
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| 2 | RP1L1, RP88
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| Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families
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| Hu YS, Song H, Li Y, Xiao ZY, Li T.
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| Int J Ophthalmol. Jun 18;12(6):915-923. doi: 10.18240/ijo.2019.06.06. 2019
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| 3 | OMACD, RP1L1, RP88
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| RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy.2013 PMID:
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| Davidson AE, Sergouniotis PI, Mackay DS, Wright GA, Waseem NH, Michaelides M, Holder GE, Robson AG, Moore AT, Plagnol V, Webster AR.
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| Hum Mutat. Mar;34(3):506-14. doi: 10.1002/humu.22264. Epub 2013 Jan 17. 2013
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