A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A-Reference-Cited by-同舟云学术

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A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A

Published:2021-04-01 Issue:6 Volume:23 Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Rep

Author:

Li Qiong¹,Liang Pengfei¹,Wang Shujuan¹,Li Wei¹,Wang Jian¹,Yang Yang¹,An Xiaogang¹,Chen Jun¹,Zha Dingjun¹

Affiliation:

1. Department of Otolaryngology‑Head and Neck Surgery, Xijing Hospital, Air Force Medical University, Xi'an, Shaanxi 710032, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 9 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. A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non‐syndromic deafness 2A in a Chinese family;Molecular Genetics & Genomic Medicine;2024-07

2. Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss;Medicine;2024-04-19

3. Comprehensive pan‑cancer analysis of potassium voltage-gated channel Q4 (KCNQ4) gene across multiple human malignant tumors;Scientific Reports;2023-10-30

4. NIDCD’s 5-Year Strategic Plan Describes Scientific Priorities and Commitment to Basic Science;Journal of the Association for Research in Otolaryngology;2023-06-21

5. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

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