Molecular Analysis of GAA Repeats and Four Linked Bi‐allelic Markers in and Around the Frataxin Gene in Patients and Normal Populations from India-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Molecular Analysis of GAA Repeats and Four Linked Bi‐allelic Markers in and Around the Frataxin Gene in Patients and Normal Populations from India

Published:2004-05 Issue:3 Volume:68 Page:189-195
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Chattopadhyay B.¹,Gupta S.¹,Gangopadhyay P. K.²,Das S. K.²,Roy T.²,Mukherjee S. C.³,Sinha K. K.⁴,Singhal B. S.⁵,Bhattacharyya N. P.

Affiliation:

1. Crystallography and Molecular Biology Division, Saha Institute of Nuclear Physics, 1/AF Bidhan Nagar, Kolkata: 700 064, India

2. Bangur Institute of Neurology, 52/1A, Sambhunath Pandit Street, Kolkata

3. Medical College Hospital, Kolkata

4. Advanced Diagnostic Centre, Ranchi

5. Bombay Hospital, Medical Research Centre, Mumbai

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1529-8817.2003.00087.x

Reference27 articles.

1. Ethnic India: A Genomic View, With Special Reference to Peopling and Structure

2. Haplotype analysis of genomic polymorphisms in and around the myotonic dystrophy locus in diverse populations of India

3. Negligible male gene flow across ethnic boundaries in India, revealed by analysis of Y‐chromosomal DNA polymorphisms;Bhattacharyya;Genome Res,1999

4. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Cited by 9 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. A Rare Phenotype of Inherited Cerebellar Ataxia;Cureus;2022-09-06

2. Familial segmental spinal myoclonus: a rare clinical feature of Friedreich’s ataxia;SpringerPlus;2015-07-08

3. Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR;European Journal of Medical Genetics;2015-03

4. Genetic Variations Creating MicroRNA Target Sites in the FXN 3′-UTR Affect Frataxin Expression in Friedreich Ataxia;PLoS ONE;2013-01-30

5. Low predisposition to instability of the Friedreich ataxia gene in Cuban population;Clinical Genetics;2010-05-09

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