Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) Mutations in a Population of Adult Cochlear Implant Candidates-Reference-Cited by-同舟云学术

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Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) Mutations in a Population of Adult Cochlear Implant Candidates

Published:2010-08 Issue:6 Volume:31 Page:919-922
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Hochman Jordan B.,Stockley Tracy L.,Shipp D.,Lin Vincent Y. W.,Chen Joseph M.,Nedzelski Julian M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference17 articles.

1. Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan China.;Xu;Ann Otol Rhinol Laryngol,2001

2. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.;Denoyelle;Hum Mol Genet,1997

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness.;Estivill;Lancet,1998

4. Impaired permeability to Ins(1,5,6) P3 in a mutant connexin underlies recessive hereditary deafness.;Beltramello;Nat Cell Biol,2005

5. Temporal bone histopathology in connexin 26 related hearing loss.;Jun;Laryngoscope,2000

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1. Evaluation of a Less Invasive Cochlear Implant Surgery in OPA1 Mutations Provoking Deafblindness;Genes;2023-03-02

2. Cochlear Health and Cochlear-implant Function;Journal of the Association for Research in Otolaryngology;2023-01-04

3. SOX9 and SOX10 control fluid homeostasis in the inner ear for hearing through independent and cooperative mechanisms;Proceedings of the National Academy of Sciences;2022-11-07

4. Kölliker’s organ-supporting cells and cochlear auditory development;Frontiers in Molecular Neuroscience;2022-10-11

5. A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear Implantation;Audiology and Neurotology;2020-09-02

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