Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss-Reference-Cited by-同舟云学术

Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss

Published:2013-07-30 Issue:7 Volume:8 Page:e69549
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Zhao Yali,Zhao Feifan,Zong Liang,Zhang Peng,Guan Liping,Zhang Jianguo,Wang Dayong,Wang Jing,Chai Wei,Lan Lan,Li Qian,Han Bing,Yang Ling,Jin Xin,Yang Weiyan,Hu Xiaoxiang,Wang Xiaoning,Li Ning,Li Yingrui,Petit Christine,Wang Jun,Wang Huanming Yang Jian,Wang Qiuju

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference18 articles.

1. Non-syndromic autosomal-dominant deafness;MB Petersen;Clin Genet,2002

2. Exome sequencing identifies the cause of a mendelian disorder;SB Ng;Nat Genet,2010

3. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells;A Adato;Hum Mol Genet,2005

4. Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9;NG Robertson;Hum Mol Genet,2001

5. Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy;DA Pillers;Mol Genet Metab,2002

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