Literature DB >> 28859437

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Zhaoxin Ma1, Wenjun Xia2, Fei Liu3, Jing Ma3, Shaoyang Sun3, Jin Zhang3, Nan Jiang3, Xu Wang3, Jiongjiong Hu1, Duan Ma2,3,4.   

Abstract

Entities:  

Year:  2017        PMID： 28859437     DOI： 10.1093/hmg/ddx232

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  4 in total

1.  A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.

Authors:  Xue Gao; Jin-Cao Xu; Wei-Qian Wang; Yong-Yi Yuan; Dan Bai; Sha-Sha Huang; Guo-Jian Wang; Yu Su; Jia Li; Dong-Yang Kang; Mei-Guang Zhang; Xi Lin; Pu Dai
Journal:  Biomed Res Int       Date:  2018-04-04       Impact factor: 3.411

2.  The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish.

Authors:  Deyong Xiao; Huijun Wang; Lili Hao; Xiao Guo; Xiaojing Ma; Yanyan Qian; Hongbo Chen; Jing Ma; Jin Zhang; Wei Sheng; Weinian Shou; Guoying Huang; Duan Ma
Journal:  PLoS Genet       Date:  2018-08-15       Impact factor: 5.917

3.  A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities.

Authors:  Dan Bai; Xudong Zhang; Yu Li; Jing Ni; Kai Lan
Journal:  Biomed Res Int       Date:  2021-06-21       Impact factor: 3.411

4.  The slc4a2b gene is required for hair cell development in zebrafish.

Authors:  Fuping Qian; Xin Wang; Zhenhua Yin; Gangcai Xie; Huijun Yuan; Dong Liu; Renjie Chai
Journal:  Aging (Albany NY)       Date:  2020-10-12       Impact factor: 5.682
  4 in total

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