Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation-Reference-Cited by-同舟云学术

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Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation

Published:2019-04-30 Issue:1 Volume:41 Page:114-124
ISSN:0196-0202
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Song Mee Hyun,Jung Jinsei,Rim John Hoon,Choi Hye Ji,Lee Hack June,Noh Byunghwa,Lee Jun Suk,Gee Heon Yung,Choi Jae Young

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference61 articles.

1. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.;Bademci;Genet Med,2016

2. Active middle ear implant compared with open-fit hearing aid in sloping high-frequency sensorineural hearing loss.;Boeheim;Otol Neurotol,2010

3. An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.;Bonnet;Eur J Hum Genet,2016

4. A novel frameshift mutation of the USH2A Gene in a Korean patient with Usher Syndrome Type II.;Boo;Clin Exp Otorhinolaryngol,2013

5. Severe to profound deafness may be associated with MYH9-related disease: report of 4 patients.;Canzi;Acta Otorhinolaryngol Ital,2016

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1. Clinical Characteristics and Audiological Profiles of Patients with Pathogenic Variants of WFS1;Journal of Clinical Medicine;2024-08-16

2. Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss;Journal of Clinical Medicine;2024-03-29

3. Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre study;Journal of Otolaryngology - Head & Neck Surgery;2023-12-15

4. Novel small molecule-mediated restoration of the surface expression and anion exchange activity of mutated pendrin causing Pendred syndrome and DFNB4;Biomedicine & Pharmacotherapy;2023-11

5. Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families;Biochemical Genetics;2023-10-01

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