Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Retinal Diseases and RP1L1[original query] |
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RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy. Human mutation 2012 Dec . Davidson AE, Sergouniotis PI, Mackay DS, Wright GA, Waseem NH, Michaelides M, Holder GE, Robson AG, Moore AT, Plagnol V, Webster AR |
[New techniques for quantification of color vision in disorders of cone function : Cambridge color test and photoreceptor-specific temporal contrast sensitivity in patients with heterozygous RP1L1 and RPGR mutations]. Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 2020 5 118 (2): 144-153. Huchzermeyer Cord, Fars Julien, Stöhr Heidi, Kremers J |
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- Page last updated:May 06, 2024
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