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Ophthalmic Genetics Volume 43, 2022 - Issue 5
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Letter to the Editor

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

Chae Yeon Leea Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaView further author information
,
Ja-Hyun Jangb Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaView further author information
,
Gyule Hana Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaView further author information
,
Tae-Young Chunga Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaView further author information
&
Dong Hui Lima Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea;c Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South KoreaCorrespondence[email protected]
View further author information
Pages 724-728 | Received 03 Jul 2021, Accepted 16 Jul 2022, Published online: 31 Aug 2022
 
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Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Additional information

Funding

This work was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea [grant number: HI19C0481 and HC19C0142], and a National Research Foundation of Korea grant funded by the Korean government’s Ministry of Education [NRF-2021R1C1C1007795; Seoul, Korea], which were received by D.H.L. The funding organizations had no role in the design or conduct of the study.

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