Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes-Reference-Cited by-同舟云学术

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Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes

Published:2013-03 Issue:3 Volume:77 Page:379-383
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Huang Shasha,Han Dongyi,Wang Guojian,Yuan Yongyi,Song Yueshuai,Han Mingyu,Chen Zhengyi,Dai Pu

Funder

National Natural Science Foundation of China

State 863 High Technology R&D Key Project of China

Ministery of Science and Technology of China

Ministery of Health of China

New Star Program of Beijing Science and Technology

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference26 articles.

1. Universal newborn hearing screening – the Colorado story;Downs;Int. J. Pediatr. Otorhinolaryngol.,1995

2. Newborn hearing screening: the great omission;Mehl;Pediatrics,1998

3. The Colorado newborn hearing screening project, 1992–1999: on the threshold of effective population-based universal newborn hearing screening;Mehl;Pediatrics,2002

4. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998

5. Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population;Gabriel;Hum. Mutat.,2001

Cited by 8 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. Genetic Determinants of Non-Syndromic Enlarged Vestibular Aqueduct: A Review;Audiology Research;2021-08-28

2. Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss;Bioscience Reports;2019-03

3. Analysis between phenotypes and genotypes of inner ear malformation;Acta Oto-Laryngologica;2019-02-14

4. Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders;Russian Journal of Genetics;2017-01

5. Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients;PLOS ONE;2016-09-14

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