Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation-Reference-Cited by-同舟云学术

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Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation

Published:2012-08-06 Issue:8 Volume:7 Page:e42463
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Bae Jae Woong,Kim Dong-Bin,Choi Jae Young,Park Hong-Joon,Lee Jong Dae,Hur Dong Gu,Bae Seung-Hyun,Jung Da Jung,Lee Sang Heun,Kim Un-Kyung,Lee Kyu Yup

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Cited by 20 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. Novel Variant of FDXR as a Molecular Etiology of Postlingual Post-synaptic Auditory Neuropathy Spectrum Disorder via Mitochondrial Dysfunction: Reiteration of the Correlation between Genotype and Cochlear Implantation Outcomes;Clinical and Experimental Otorhinolaryngology;2024-08-31

2. High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect;Scientific Reports;2024-07-03

3. Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss;Journal of Korean Medical Science;2023

4. Searching for the Molecular Basis of Partial Deafness;International Journal of Molecular Sciences;2022-05-27

5. Diagnosis and Intervention of Genetic Hearing Loss;Journal of Clinical Otolaryngology Head and Neck Surgery;2021-06

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