<i>GJB2</i> Mutations and Genotype-Phenotype Correlation in 335 Patients from Germany with Nonsyndromic Sensorineural Hearing Loss: Evidence for Additional Recessive Mutations Not Detected by Current Methods-Reference-Cited by-同舟云学术

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GJB2 Mutations and Genotype-Phenotype Correlation in 335 Patients from Germany with Nonsyndromic Sensorineural Hearing Loss: Evidence for Additional Recessive Mutations Not Detected by Current Methods

Published:2010 Issue:6 Volume:15 Page:375-382
ISSN:1420-3030
Container-title:Audiology and Neurotology
language:en
Short-container-title:Audiol Neurotol

Author:

Bartsch O.,Vatter A.,Zechner U.,Kohlschmidt N.,Wetzig C.,Baumgart A.,Nospes S.,Haaf T.,Keilmann A.

Publisher

S. Karger AG

Subject

Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology

Cited by 23 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. Genetic analysis of 106 sporadic cases with hearing loss in the UAE population;Human Genomics;2024-06-07

2. Genetic etiology of non-syndromic hearing loss in Europe;Human Genetics;2022-01-19

3. Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center;Ear & Hearing;2021-11-08

4. Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate;Egyptian Journal of Medical Human Genetics;2021-05-07

5. Frühe Prädiktoren der Sprachentwicklung von Kindern mit permanenter Hörstörung;Kindheit und Entwicklung;2021-01

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