Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities-Reference-Cited by-同舟云学术

Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities

Published:2007-12-13 Issue:3 Volume:13 Page:172-181
ISSN:1420-3030
Container-title:Audiology and Neurotology
language:en
Short-container-title:Audiol Neurotol

Author:

Wu Chen-Chi,Chen Pei-Jer,Chiu Yu-Hsun,Lu Ying-Chang,Wu Ming-Chueh,Hsu Chuan-Jen

Publisher

S. Karger AG

Subject

Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology

Reference39 articles.

1. Prevalent connexin 26 gene (GJB2) mutations in Japanese

2. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

3. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

4. Diagnostic Yield of High-Resolution Computed Tomography for Pediatric Sensorineural Hearing Loss

5. Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

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