The clinical features of patients with the homozygous 235delC and the compound-heterozygous Y136X/G45E of the GJB2 mutations (Connexin 26) in cochlear implant recipients-Reference-Cited by-同舟云学术

The clinical features of patients with the homozygous 235delC and the compound-heterozygous Y136X/G45E of the GJB2 mutations (Connexin 26) in cochlear implant recipients

Published:2011-08 Issue:4 Volume:38 Page:444-449
ISSN:0385-8146
Container-title:Auris Nasus Larynx
language:en
Short-container-title:Auris Nasus Larynx

Author:

Yoshikawa Satoko,Kawano Atsushi,Hayashi Chieri,Nishiyama Nobuhiro,Kawaguchi Sachie,Furuse Hiroko,Ikeda Katsuhisa,Suzuki Mamoru,Nakagawa Masahumi

Publisher

Elsevier BV

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference23 articles.

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2. Nonsyndromic hearing impairment: unparalleled heterogeneity;Van Camp;Am J Hum Genet,1997

3. A new era in the genetics of deafness;Steel;N Engl J Med,1998

4. Progress in understanding GJB2-linked deafness;Gualandi;Community Genet,2003

5. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness;Kelsell;Nature,1997

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2. Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population;PLOS ONE;2015-06-10

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

4. Prediction of cochlear implant performance by genetic mutation: The spiral ganglion hypothesis;Hearing Research;2012-10

5. GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss.;Current Genomics;2011-11-01