Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment-Reference-Cited by-同舟云学术

Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

Published:2012-02-28 Issue:2 Volume:7 Page:e30720
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Yuan Yongyi,Zhang Xun,Huang Shasha,Zuo Lujie,Zhang Guozheng,Song Yueshuai,Wang Guojian,Wang Hongtian,Huang Deliang,Han Dongyi,Dai Pu

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference60 articles.

1. Epidemiology, etiology and genetic patterns.;MM Cohen,1995

2. Hereditary Hearing Loss website.

3. Strengthen the research on prevention and treatment of sensorineural hearing loss in China.;DY Han;Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi,2010

4. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.;Y Yuan;J Transl Med,2009

5. Connexin-26 mutations in sporadic and inherited sensorineural deafness.;X Estivill;Lancet,1998

Cited by 28 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. 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

2. Gene Screening for Non-Syndromic Deafness in Hainanese Patients;The Journal of International Advanced Otology;2023-08-01

3. Cross-Sectional Study to Estimate the Prevalence of Inner-Ear Anomalies in Children With Congenital Sensorineural Hearing Loss by High-Resolution Computed Tomography (HRCT) Temporal Bone Scan;Cureus;2023-07-19

4. ANALYSIS OF THE C.757A>G P.(ILE253VAL) VARIANT OF THE SLC26A4 GENE IN GJB2-NEGATIVE PATIENTS WITH HEARING LOSS IN YAKUTIA;YAKUT MED J;2023

5. Molecular screening of patients with profound hearing loss from Chengdu, China;Acta Oto-Laryngologica;2021-12-22