Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation-Reference-Cited by-同舟云学术

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Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation

Published:2004-08 Issue:8 Volume:68 Page:995-1005
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Mesolella Massimo,Tranchino Gaetano,Nardone Massimiliano,Motta Sergio,Galli Vieri

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference37 articles.

1. A genetic approach to understanding inner ear function;Battey;J. Clin. Invest.,2000

2. Boothroyd et al., Clinical implication of Coclear impiants in children, Ear Hear. 12 (1993) 81–89.

3. Likage studies of non syndromic recessive deafness (NSRD) in a family originating from Mirpur region of Pakistan maps DFNB1 centromeric to D13S175;Brown;Hum. Mol. Gen.,1996

4. Clinical studies of families with hearing loss attributable to mutations in the Connexin 26 gene (GJB2/DFNB1);Cohn;Pediatrics,1999

5. Dong et al., Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews, Mol. Gene. Metab. 73 (2001) 160–163.

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. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29

2. Effect of GJB2 235delC and 30-35delG genetic polymorphisms on risk of congenital deafness in a Chinese population;Genetics and Molecular Research;2017

3. GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype;The Laryngoscope;2013-10-08

4. Long term speech perception after cochlear implant in pediatric patients with GJB2 mutations;Auris Nasus Larynx;2013-10

5. A Novel MYO6 Splice Site Mutation Causes Autosomal Dominant Sensorineural Hearing Loss Type DFNA22 with a Favourable Outcome after Cochlear Implantation;Audiology and Neurotology;2013

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