Rescue of the Congenital Hereditary Endothelial Dystrophy Mouse Model by Adeno-Associated Virus–Mediated Slc4a11 Replacement
Author:
Funder
NIH
Knights Templar Eye Foundation
NCATS
Publisher
Elsevier BV
Subject
General Materials Science
Reference35 articles.
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4. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2);Vithana;Nat Genet,2006
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1. Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy;Orphanet Journal of Rare Diseases;2022-09-17
2. Mitochondrial ROS in Slc4a11 KO Corneal Endothelial Cells Lead to ER Stress;Frontiers in Cell and Developmental Biology;2022-04-26
3. The H+ Transporter SLC4A11: Roles in Metabolism, Oxidative Stress and Mitochondrial Uncoupling;Cells;2022-01-07
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