Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11-Reference-Cited by-同舟云学术

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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

Published:2006-07-06 Issue:1 Volume:44 Page:64-68
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Jiao X.,Sultana A.,Garg P.,Ramamurthy B.,Vemuganti G. K,Gangopadhyay N.,Hejtmancik J F.,Kannabiran C.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 97 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms;Progress in Retinal and Eye Research;2024-09

2. Aquaporins in the Cornea;International Journal of Molecular Sciences;2024-03-28

3. Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells;PLOS ONE;2024-01-22

4. Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy;Translational Vision Science & Technology;2023-10-03

5. Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy;Frontiers in Medicine;2023-06-27

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