Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation-Reference-Cited by-同舟云学术

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Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation

Published:2004-11 Issue:6 Volume:25 Page:935-942
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:Otology & Neurotology

Author:

Sinnathuray Arasa Raj,Toner Joseph G.,Clarke-Lyttle Joanne,Geddis Andrea,Patterson Christopher C.,Hughes Anne E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Sensory Systems,Otorhinolaryngology

Reference27 articles.

1. Molecular Diagnosis of Deafness: Impact of Gene Identification

2. Genetics, genomics and gene discovery in the auditory system

3. Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

4. A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

5. Gap junction systems in the mammalian cochlea

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1. The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates;European Journal of Human Genetics;2024-03-15

2. The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates;2024-01-17

3. Predictors of Early Language Outcomes in Children with Connexin 26 Hearing Loss across Three Countries;Children;2022-07-01

4. Novel Cellular Stress Models with Implications in Understanding and Treating ENT Pathologies;Biomedical Translational Research;2022

5. Pediatric Otologic Surgery;Cummings Pediatric Otolaryngology;2021

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