Associated Papers
Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to RP1 Truncations: Confirmation, Refinement, and Questions.
Wang J et al.
Frontiers in Cell and Developmental Biology, 2021
33681214 (PubMed )
Supplement: Table_4.XLSX › Sheet1
Expanding the retinal phenotype of RP1: from retinitis pigmentosa to a novel and singular macular dystrophy.
Riera M et al.
The British Journal of Ophthalmology, 2020
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia.
Chassine T et al.
The British Journal of Ophthalmology, 2015
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