Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province-Reference-Cited by-同舟云学术

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Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province

Published:2019-01-28 Issue:3 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Zhou Yongan¹,Li Chao²^ORCID,Li Min²,Zhao Zhonghua³,Tian Shuxiong²,Xia Hou²,Liu Peixian¹,Han Yaxin²,Ren Ruirui²,Chen Jianping²,Jia Caihong¹,Guo Wei⁴

Affiliation:

1. Shanxi Medical University Second Affiliated Hospital Taiyuan Shanxi China

2. The Graduate School Shanxi Medical University Taiyuan Shanxi China

3. Institute of Biomedical Sciences Shanxi University Taiyuan Shanxi China

4. Xinzhou Traditional Chinese Medicine Hospital Xinzhou Shanxi China

Funder

Shanxi Province science and technology Foundation Research Grant

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.537

Reference28 articles.

1. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India

2. Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G

3. A commonSLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct

4. Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

5. Noninvasive test for mitochondrial DNA A1555G mutation associated with deafness;Fan W.;Clinical Laboratory,2017

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3. The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control Study;Pharmacogenomics and Personalized Medicine;2024-03

4. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China;BMC Medical Genomics;2024-02-20

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