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Compound heterozygous mutations in the SLC4A11 gene associated with congenital hereditary endothelial dystrophy in a Chinese family

  • Published:2022-03-16 Issue:4 Volume:43 Page:538-542
  • ISSN:1381-6810
  • Container-title:Ophthalmic Genetics
  • language:en
  • Short-container-title:Ophthalmic Genetics

Author:

Liu Min12,Xia Jia-Li1,Yang Hong3,Yu Ling13ORCID

Affiliation:

1. Department of Ophthalmology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, China

2. Department of Ophthalmology, The People’s Hospital of Wenjiang Chengdu, Chengdu, Sichuan Province, China

3. Department of Ophthalmology, Daping Hospital, Army Medical Center, Army Medical University, Chongqing, Shapingba, China

Funder

Affiliated Hospital of Southwest Medical University

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Cited by 2 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. Corneal transplantation in children - when and how?;Expert Review of Ophthalmology;2023-01-02

2. Updates on congenital hereditary endothelial dystrophy;Taiwan Journal of Ophthalmology;2023
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