Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing Rehabilitation-Reference-Cited by-同舟云学术

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Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing Rehabilitation

Published:2021-01-06 Issue:3 Volume:42 Page:644-653
ISSN:1538-4667
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Lee Sang-Yeon,Han Seung Cheol,Han Jin Hee,Kim Min Young,Oh Doo-Yi,Kim Namju Justin,Song Jae-Jin,Koo Ja-Won,Lee Jun Ho,Oh Seung-Ha,Choi Byung Yoon

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference28 articles.

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

2. GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype.;Chan;Laryngoscope,2014

3. Prediction model for audiological outcomes in patients with GJB2 mutations.;Chen;Ear Hear,2020

4. Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.;Choi;J Clin Invest,2011

5. Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?;Choi;Hum Mutat,2009

Cited by 6 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. Clinical characteristics and hearing loss etiology of cochlear implantees undergoing surgery in their teens, 20s, and 30s;European Archives of Oto-Rhino-Laryngology;2024-05-27

2. Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up;International Journal of Molecular Sciences;2023-11-25

3. Genetic Load of Alternations of Transcription Factor Genes in Non-Syndromic Deafness and the Associated Clinical Phenotypes: Experience from Two Tertiary Referral Centers;Biomedicines;2022-08-30

4. Full etiologic spectrum of pediatric severe to profound hearing loss of consecutive 119 cases;Scientific Reports;2022-07-19

5. Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants;Ear & Hearing;2022-06-17

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