Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population-Reference-Cited by-同舟云学术

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Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population

Published:2024-03-01 Issue:3 Volume:28 Page:123-130
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Tang Xianfa¹²³^ORCID,Cheng Hui¹²³,Cheng Lu¹²³,Liang Bo¹²³,Chen Mengyun¹²³,Zheng Xiaodong¹²³,Xiao Fengli¹²³

Affiliation:

1. Department of Dermatology and Institute of Dermatology at No. 1 Hospital, Anhui Medical University, Hefei, China.

2. Key Laboratory of Dermatology, Ministry of Education, Hefei, China.

3. Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, Hefei, China.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2023.0027

Reference37 articles.

1. An integrated map of genetic variation from 1,092 human genomes

2. Functional Characterization of Novel Human and Mouse Equilibrative Nucleoside Transporters (hENT3 and mENT3) Located in Intracellular Membranes

3. Genome-Wide Association of PVT1 with Vitiligo

4. Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect

5. Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis

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