SLC44A4mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

SLC44A4mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

Published:2016-12-23 Issue: Volume: Page:ddw394
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Ma Zhaoxin,Xia Wenjun,Liu Fei,Ma Jing,Sun Shaoyang,Zhang Jin,Jiang Nan,Wang Xu,Hu Jiongjiong,Ma Duan

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/2/383/18399093/ddw394.pdf

Reference43 articles.

1. Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology

2. A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3;Chatterjee;Hum. Genet,2009

3. Missense mutations inPOU4F3cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding

4. An electric lobe suppressor for a yeast choline transport mutation belongs to a new family of transporter-like proteins

5. Isoforms, Expression, Glycosylation, and Tissue Distribution of CTL2/SLC44A2

Cited by 8 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. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

2. Genome-Wide Integrative Transcriptional Profiling Identifies Age-Associated Signatures in Dogs;Genes;2023-05-23

3. The Roles of Solute Carriers in Auditory Function;Frontiers in Genetics;2022-01-26

4. Fine-Scale Genetic Structure and Natural Selection Signatures of Southwestern Hans Inferred From Patterns of Genome-Wide Allele, Haplotype, and Haplogroup Lineages;Frontiers in Genetics;2021-08-24

5. The effect of season of birth on brain epigenome-wide DNA methylation of older adults;Journal of Developmental Origins of Health and Disease;2021-07-26

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3