SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss-Reference-Cited by-同舟云学术

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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Published:2008-08 Issue:8 Volume:10 Page:586-592
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Dai Pu,Li Qi,Huang Deliang,Yuan Yongyi,Kang Dongyang,Miller David T.,Shao Hong,Zhu Qingwen,He Jia,Yu Fei,Liu Xin,Han Bing,Yuan Huijun,Platt Orah S.,Han Dongyi,Wu Bai-Lin

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference28 articles.

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

Cited by 53 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. CRISPR/Cas9-mediated exon skipping to restore premature translation termination in a DFNB4 mouse model;Gene Therapy;2024-09-04

2. 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

3. Carrier frequencies, trends, and geographical distribution of hearing loss variants in China: The pooled analysis of 2,161,984 newborns;Heliyon;2024-02

4. Optimized concurrent hearing and genetic screening in Beijing, China: A cross-sectional study;BioScience Trends;2023-04-30

5. Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia);Genes;2023-04-17

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