Prevalence of GJB2 and TECTA gene mutations in children with non-syndromic hearing loss visiting an Otorhino-laryngology Hospital in Ho Chi Minh City, Viet Nam-Reference-Cited by-同舟云学术

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Prevalence of GJB2 and TECTA gene mutations in children with non-syndromic hearing loss visiting an Otorhino-laryngology Hospital in Ho Chi Minh City, Viet Nam

Published:2023-01-31 Issue:1 Volume:10 Page:5523-5529
ISSN:2198-4093
Container-title:Biomedical Research and Therapy
language:en
Short-container-title:Biomed. Res. Ther.

Author:

Hoang Phuong Thu Vu,Ngo Minh Xuan,Tran Quang Minh Le,Nguyen Thanh Vinh,Do Hong Giang,Nguyen Thanh Vu,Nguyen Anh Thu Ha,Do Thi Thu Hang,Huynh Thi Dieu Hien,Tran Phan Chung Thuy

Publisher

Biomedical Research and Therapy

Subject

General Biochemistry, Genetics and Molecular Biology

Cited by 1 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 treatment-focused approach to medical investigations for hearing loss in infants;Journal of the Royal Society of New Zealand;2024-09-11

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