A Novel Mutation Located in the N‐Terminal Domain of <scp>MYO15A</scp> Caused Sensorineural Hearing Loss
Our study demonstrates that the novel variant c.2482C>T in the MYO15A gene may cause inner ear hair cell dysfunction and audiological disorders in this family.
Authors
- Shihong Duan
- Xingjian Chen (ORCID: https://orcid.org/0000-0001-9639-1584)
- Jiong Dang
- Min‐Xin Guan (ORCID: https://orcid.org/0000-0001-5067-6736)
- Yufen Guo (ORCID: https://orcid.org/0000-0002-4650-5237)
- Zhipeng Nie
- Zengping Liu (ORCID: https://orcid.org/0000-0002-2578-293X)
- Baicheng Xu (ORCID: https://orcid.org/0000-0002-9291-9369)
- Yong Li (ORCID: https://orcid.org/0000-0001-7956-9600)
- Yanli Wang (ORCID: https://orcid.org/0000-0002-5969-1745)
- Yiming Zhu (ORCID: https://orcid.org/0000-0003-2353-5713)
- Huan Tan
Institutions
- Lanzhou University Second Hospital (CN)
- Zhejiang University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2024-12-01
- DOI
- https://doi.org/10.1002/mgg3.70042
- Citations
- 2
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 0.72
Funders
- Lanzhou University
- National Natural Science Foundation of China
- Natural Science Foundation of Gansu Province