Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy-Reference-Cited by-同舟云学术

Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy

Published:2023-10-02 Issue:19 Volume:133 Page:
ISSN:1558-8238
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Kabra Meha,Shahi Pawan K.,Wang Yuyuan,Sinha Divya,Spillane Allison,Newby Gregory A.^ORCID,Saxena Shivani,Tong Yao,Chang Yu,Abdeen Amr A.,Edwards Kimberly L.,Theisen Cole O.,Liu David R.^ORCID,Gamm David M.^ORCID,Gong Shaoqin,Saha Krishanu^ORCID,Pattnaik Bikash R.^ORCID

Funder

National Institute of Health, McPherson Eye Research Institute and Retina research foundation, Gund-Harrington Scholar, Research to Prevent Blindness, Helen Hay Whitney Foundation, HHMII

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/171356/files/pdf

Reference53 articles.

1. Focus on Kir7.1: physiology and channelopathy

2. Sensing through Non-Sensing Ocular Ion Channels

3. Characterization of the R162W Kir7.1 mutation associated with snowflake vitreoretinopathy

4. Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish

5. Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis

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