A <scp><i>KCNQ4</i></scp> Gene Variant (c.<scp>701A</scp> > G; p.<scp>His234Arg</scp>) in a Chinese Family With Nonsyndromic Deafness <scp>2A</scp>
This family has autosomal dominant nonsyndromic hereditary hearing loss caused by a variation in the KCNQ4 gene, characterized by high-frequency hearing loss.
Authors
- Chengcheng Huang (ORCID: https://orcid.org/0009-0009-5879-1689)
- Jingyuan Cao
- Yi Sun (ORCID: https://orcid.org/0000-0003-1890-5599)
- Chih‐Chao Yang (ORCID: https://orcid.org/0000-0002-0352-3144)
- Yi‐Ming Ji
- Guang Yang (ORCID: https://orcid.org/0000-0001-8622-2146)
- R. Chen
- Yu Lu (ORCID: https://orcid.org/0000-0003-3944-1252)
- Guo‐Qing Gong (ORCID: https://orcid.org/0000-0003-1669-4185)
- LiWang
- Zhao Zhang (ORCID: https://orcid.org/0000-0002-1133-4191)
- Jin Huang (ORCID: https://orcid.org/0000-0003-1997-6161)
- Yunyun Yang
- Huifang Lü
Institutions
- Sichuan University (CN)
- Courant Institute of Mathematical Sciences (US)
- West China Hospital of Sichuan University (CN)
- Tongren Hospital (CN)
- Wuhan Third Hospital (CN)
- Central Hospital of Wuhan (CN)
- General Hospital of Central Theater Command
- Huazhong University of Science and Technology (CN)
- New York University (US)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1002/mgg3.70075
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Hubei Province