The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China-Reference-Cited by-同舟云学术

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The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China

Published:2020-09 Issue: Volume:136 Page:110143
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Liu Xiao-Wen,Wang Jian-Chao,Wang Su-Yang,Li Shu-Juan,Zhu Yi-Ming,Ding Wen-Juan,Xu Chen-Yang,Duan Lei,Xu Bai-Cheng,Guo Yu-Fen

Funder

National Natural Science Foundation of China

Lanzhou University

Gansu Provincial Health Industry Research Plan Project

Gansu Provincial Youth Science and Technology

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Genetics of hearing and deafness;Angeli;Anat. Rec. (Hoboken),2012

2. A note on deaf mutism;Chung;Ann. Hum. Genet.,1959

3. Newborn hearing screening -- A silent revolution;Morton;N. Engl. J. Med.,2006

4. A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss;Du;Genomics,2014

Cited by 13 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. In Utero Gene Therapy and its Application in Genetic Hearing Loss;Advanced Biology;2024-07-15

2. Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants;Molecular Genetics & Genomic Medicine;2024-06

3. Establishment and application of a reverse dot blot assay for 13 mutations of hearing-loss genes in primary hospitals in China;Asian Biomedicine;2024-02-01

4. Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China;International Journal of Pediatric Otorhinolaryngology;2024-01

5. Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow‐up;Molecular Genetics & Genomic Medicine;2023-12

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