GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness-Reference-Cited by-同舟云学术

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GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness

Published:2015-06-29 Issue:6 Volume:273 Page:1393-1398
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Chen Kaitian,Sun Liang,Zong Ling,Wu Xuan,Zhan Yuan,Dong Chang,Cao Hui,Tang Haocheng,Jiang Hongyan

Funder

National Basic Research Program of China

National Natural Science fund of China

Minster of Health of China

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s00405-015-3693-7.pdf

Reference24 articles.

1. Haberkamp TJ, Tanyeri HM (1999) Management of idiopathic sudden sensorineural hearing loss. Am J Otol 20(587–92):593–595

2. Ogasawara H, Morimoto K, Ishii K et al (1993) A statistical analysis of sudden deafness. Nihon Jibiinkoka Gakkai Kaiho 96:914–921

3. Yildiz Z, Ulu A, Incesulu A et al (2008) The importance of thrombotic risk factors in the development of idiopathic sudden hearing loss. Clin Appl Thromb Hemost 14:356–359

4. Lin RJ, Krall R, Westerberg BD et al (2012) Systematic review and meta-analysis of the risk factors for sudden sensorineural hearing loss in adults. Laryngoscope 122:624–635

5. Uchida Y, Sugiura S, Ando F et al (2010) Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss. Laryngoscope 120:791–795

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1. Deafness gene screening based on a multilevel cascaded BPNN model;BMC Bioinformatics;2023-02-20

2. A review of bilateral sudden sensorineural hearing loss in pediatric patients;International Journal of Pediatric Otorhinolaryngology;2023-02

3. Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing;Gene;2022-04

4. Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel;Genetics in Medicine;2019-11

5. Hereditary bilateral sudden sensorineural hearing loss;Bratislava Medical Journal;2019

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