Sudden hearing loss in a family with GJB2 related progressive deafness-Reference-Cited by-同舟云学术

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Sudden hearing loss in a family with GJB2 related progressive deafness

Published:2008-11 Issue:11 Volume:72 Page:1735-1740
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Kokotas Haris,Theodosiou Maria,Korres George,Grigoriadou Maria,Ferekidou Elisabeth,Giannoulia-Karantana Aglaia,Petersen Michael B.,Korres Stavros

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Genetic epidemiology of hearing impairment;Morton;Ann. N.Y. Acad. Sci.,1991

2. Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum. Mol. Genet.,1997

3. Genes responsible for human hereditary deafness: symphony of a thousand;Petit;Nat. Genet.,1996

4. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene;Denoyelle;Hum. Mol. Genet.,1997

5. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss;Kelley;Am. J. Hum. Mutat.,1998

Cited by 12 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. Unusual phenotype in 35delG mutation: a case report;Journal of Medical Case Reports;2024-05-12

2. A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss;The Laryngoscope;2024-01-25

3. Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss;Journal of Personalized Medicine;2022-11-04

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

5. DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes;Frontiers in Molecular Neuroscience;2017-12-22

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