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A Pro23His Mutation Alters Prenatal Rod Photoreceptor Morphology in a Transgenic Swine Model of Retinitis Pigmentosa

PURPOSE. Functional studies have detected deficits in retinal signaling in asymptomatic children from families with inherited autosomal dominant retinitis pigmentosa (RP). Whether retinal abnormalities are present earlier during gestation or shortly after birth in a subset of children with autosomal...

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Detalhes bibliográficos
Main Authors: Scott, Patrick A., Fernandez de Castro, Juan P., Kaplan, Henry J., McCall, Maureen A.
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4004442/
https://ncbi.nlm.nih.gov/pubmed/24618321
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.13-13723
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