A Case of Corneal Dysplasia with Identification of POLH Gene Variants in Xeroderma Pigmentosum-Reference-Cited by-同舟云学术

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A Case of Corneal Dysplasia with Identification of POLH Gene Variants in Xeroderma Pigmentosum

Published:2019 Issue:4 Volume:60 Page:380
ISSN:0378-6471
Container-title:Journal of the Korean Ophthalmological Society
language:ko
Short-container-title:J Korean Ophthalmol Soc

Author:

Shin Eun Hae¹,Lim Dong Hui¹²,Kim Yoon-Duck¹,Woo Kyung In¹,Han Jisang³,Park Jong Eun⁴,Chung Tae-Young¹,Ki Chang-Seok⁴

Affiliation:

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

2. Department of Preventive Medicine, Graduate School, The Catholic University of Korea, Seoul, Korea.

3. Department of Medicine, Graduate School, Kyung Hee University, Seoul, Korea.

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

Publisher

Korean Ophthalmological Society

Subject

Ophthalmology

Link

https://synapse.koreamed.org/pdf/10.3341/jkos.2019.60.4.380

Reference15 articles.

1. Ocular Manifestations of Xeroderma Pigmentosum

2. Corneal Changes in Xeroderma Pigmentosum: A Clinicopathologic Report

3. Xeroderma pigmentosum

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. Xeroderma Pigmentosum in a Pediatric Patient with a Progressive Pterygium-like Lesion;Journal of the Korean Ophthalmological Society;2021-01-15

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