A Novel Connexin 26 Compound Heterozygous Mutation Results in Deafness
Author:
Affiliation:
1. Department of Otolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, U.S.A.
Funder
Toohill Research Fund of the Department of Otolaryngology and Communication Sciences, the General Clinical Research Center
NIH/NIDCD
Publisher
Wiley
Subject
Otorhinolaryngology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1097/00005537-200207000-00003
Reference27 articles.
1. Genetic Epidemiology of Hearing Impairment
2. Carrier Rates in the Midwestern United States for GJB2 Mutations Causing Inherited Deafness
3. RabionetR GaspariniP EstivillX.Connexins and Deafness Web site. Available at:http://www.iro.es/cx26deaf.html. Accessed August 2001.
4. The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population
5. Connexin 26 as a Cause of Hereditary Hearing Loss
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2. Novel deleterious mutation in MYO7A, TH and EVC2 in two Pakistani brothers with familial deafness;Pakistan Journal of Medical Sciences;2019-01-22
3. Dysfunctions of the Diffusional Membrane Pathways Mediated Hemichannels in Inherited and Acquired Human Diseases;Current Vascular Pharmacology;2009-10-01
4. Cx26 Gene Mutations in Idiopathic Progressive Hearing Loss;The Journal of Otolaryngology;2005
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