Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates

Published:2007-12 Issue:4 Volume:11 Page:455-458
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Bouwer Sonja¹,Angelicheva Dora¹,Chandler David¹,Seeman Pavel²,Tournev Ivailo³,Kalaydjieva Luba¹

Affiliation:

1. Western Australian Institute for Medical Research and Centre for Medical Research, The University of Western Australia, Perth, Australia.

2. Department of Child Neurology, DNA Laboratory, 2nd School of Medicine, Charles University, Prague, Czech Republic.

3. Department of Neurology, Medical University, Sofia, Bulgaria.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2007.0048

Reference19 articles.

1. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

2. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness

4. Carrier Rates in the Midwestern United States for GJB2 Mutations Causing Inherited Deafness

Cited by 35 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. The Iberian Roma Population Variant Server (IRPVS);Journal of Genetics and Genomics;2024-07

2. The Iberian Roma genetic variant server; population structure, susceptibility to disease and adaptive traits;2023-08-25

3. A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people;Frontiers in Medicine;2023-02-08

4. Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment;Genes;2023-02-03

5. Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene;Genes;2022-12-26

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