A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss-Reference-Cited by-同舟云学术

A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

Published:2014-02-21 Issue:2 Volume:9 Page:e89240
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Su Yu,Tang Wen-Xue,Gao Xue,Yu Fei,Dai Zhi-Yao,Zhao Jian-Dong,Lu Yu,Ji Fei,Huang Sha-Sha,Yuan Yong-Yi,Han Ming-Yu,Song Yue-Shuai,Zhu Yu-Hua,Kang Dong-Yang,HAN Dong-Yi,Dai Pu

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference46 articles.

1. Human nonsyndromic sensorineural deafness;TB Friedman;Annu Rev Genomics Hum Genet,2003

2. Genetics of deafness;KP Steel;Curr Opin Neurobiol,1996

3. Hearing loss in children with very low birth weight: current review of epidemiology and pathophysiology;R Cristobal;Arch Dis Child Fetal Neonatal Ed,2008

4. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families;F Alasti;Int J Pediatr Otorhinolaryngol,2008

5. Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer;RW Collin;Eur J Hum Genet,2008

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1. Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA;Human Molecular Genetics;2024-04-27

2. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

3. The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss;Genes;2019-09-24

4. Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls;European Journal of Human Genetics;2019-09-20

5. TECTA Gene Function and Hearing Loss : A Review;World Family Medicine Journal/Middle East Journal of Family Medicine;2017-10