Diffuse Outer Layer Opacification: A Novel Finding in Patients With Autosomal Recessive Bestrophinopathy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
Reference29 articles.
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2. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium;Marmorstein;Proc Natl Acad Sci U S A,2000
3. Bestrophin-1 influences transepithelial electrical properties and Ca2+ signaling in human retinal pigment epithelium;Marmorstein;Mol Vis,2015
4. TREK-1 and Best1 channels mediate fast and slow glutamate release in astrocytes upon GPCR activation;Woo;Cell,2012
5. Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy;Davidson;Invest Ophthalmol Vis Sci,2011
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1. A Review of Current and Prospective Treatments for Channelopathies, with a Focus on Gene and Protein Therapy;Current Pharmaceutical Design;2023-05
2. Twelve-year follow up of a case of autosomal recessive bestrophinopathy with transient resolution of retinal edema in one eye;European Journal of Ophthalmology;2022-01-06
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