Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference25 articles.
1. New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p
2. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
3. Connexin 26 gene linked to a dominant deafness
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2. Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss;Annals of Human Genetics;2018-09-03
3. Long Term Speech Perception Outcomes of Cochlear Implantation in Gap Junction Protein Beta 2 Related Hearing Loss;Journal of Audiology and Otology;2017-07-31
4. Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic);PLOS ONE;2016-05-25
5. The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis;Human Genetics;2016-01-09
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