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Retinal Dystrophy Associated With RLBP1 Retinitis Pigmentosa: A Five-Year Prospective Natural History Study

PURPOSE: To assess the progression in functional and structural measures over a five-year period in patients with retinal dystrophy caused by RLBP1 gene mutation. METHODS: This prospective, noninterventional study included patients with biallelic RLBP1 mutations from two clinical sites in Sweden and...

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Detalles Bibliográficos
Autores principales:	Burstedt, Marie, Whelan, James H., Green, Jane S., Holopigian, Karen, Spera, Claudio, Greco, Erin, Deslandes, Jean-Yves, Wald, Michael, Grosskreutz, Cynthia, Ni, Xiao, Normand, Guillaume, Maker, Michael, Charil, Arnaud, Rosol, Michael, He, Yunsheng, Stasi, Kalliopi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Association for Research in Vision and Ophthalmology 2023
Materias:	Retina
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615144/ https://www.ncbi.nlm.nih.gov/pubmed/37883093 http://dx.doi.org/10.1167/iovs.64.13.42

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