Unilateral posterior polymorphous corneal dystrophy due to a novel <i>ZEB1</i> gene mutation in a Korean girl-Reference-Cited by-同舟云学术

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Unilateral posterior polymorphous corneal dystrophy due to a novel ZEB1 gene mutation in a Korean girl

Published:2022-08-31 Issue:5 Volume:43 Page:724-728
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Lee Chae Yeon¹,Jang Ja-Hyun²,Han Gyule¹,Chung Tae-Young¹,Lim Dong Hui¹³

Affiliation:

1. Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

2. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

3. Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea

Funder

Korea Health Technology

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2106495

Reference11 articles.

1. IC3D Classification of Corneal Dystrophies—Edition 2

2. The Clinical Features and Progression of the Disease in Posterior Polymorphous Corneal Dystrophy (PPCD)

3. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

4. Mutational Spectrum of theZEB1Gene in Corneal Dystrophies Supports a Genotype–Phenotype Correlation

5. EyeWiki. AAoO. Posterior polymorphous corneal dystrophy. 2020 Dec 20.

Cited by 1 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. 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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