Multimodal imaging and genetic characteristics of autosomal recessive bestrophinopathy-Reference-Cited by-同舟云学术

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Multimodal imaging and genetic characteristics of autosomal recessive bestrophinopathy

Published:2024-06 Issue:6 Volume:47 Page:104097
ISSN:0181-5512
Container-title:Journal Français d'Ophtalmologie
language:en
Short-container-title:Journal Français d'Ophtalmologie

Author:

Tekin K.,Dulger S.C.,Horozoglu Ceran T.,Inanc M.,Ozdal P.C.,Teke M.Y.

Publisher

Elsevier BV

Reference21 articles.

1. The spectrum of ocular phenotypes caused by mutations in the BEST1 gene;Boon;Prog Retin Eye Res,2009

2. Bestrophin 1 and retinal disease;Johnson;Prog Retin Eye Res,2017

3. The vitelliform macular dystrophy protein defines a new family of chloride channels;Sun;Proc Natl Acad Sci U S A,2002

4. Structure and insights into the function of a Ca(2+)-activated Cl(-) channel;Dickson;Nature,2014

5. Biallelic mutation of BEST1 causes a distinct retinopathy in humans;Burgess;Am J Hum Genet,2008

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