A Splicing Mutation in <i>Slc4a5</i> Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction

A Splicing Mutation in <i>Slc4a5</i> Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction

Fluid and solute transporters of the retinal pigment epithelium (RPE) are core components of the outer blood–retinal barrier. Characterizing these transporters and their role in retinal homeostasis may provide insights into ocular function and disease. Here, we describe RPE defects in <i>tvrm7...

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Bibliographic Details
Main Authors: Gayle B. Collin, Lanying Shi, Minzhong Yu, Nurten Akturk, Jeremy R. Charette, Lillian F. Hyde, Sonia M. Weatherly, Martin F. Pera, Jürgen K. Naggert, Neal S. Peachey, Patsy M. Nishina, Mark P. Krebs
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:International Journal of Molecular Sciences
Subjects:
sensitized chemical mutagenesis screen
mouse genetics
inherited retinal disease
retinal dysplasia
Online Access:https://www.mdpi.com/1422-0067/23/4/2220

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