Laminopathies in Russian families
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01045.x/fullpdf
Reference25 articles.
1. Lamin gene mutations in dilated cardiomyopathy;Zakliaz’minskaia;Kardiologiia (Rus),2005
2. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy;Raffaele Di Barletta;Am J Hum Genet,2000
3. Mutation analysis of the lamin A/C gene (LMNA) with different cardiomuscular phenotypes;Vytopil;J Med Genet,2003
4. Functional consequences of an LMNA mutation with a new cardiac and non-cardiac phenotype;Charniot;Hum Mutat,2003
5. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B);Muchir;Hum Mol Genet,2000
Cited by 7 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. Active microrheology using pulsed optical tweezers to probe viscoelasticity of Lamin A towards diagnosis of laminopathies;2021-02-06
2. An elderly-onset limb girdle muscular dystrophy type 1B (LGMD1B) with pseudo-hypertrophy of paraspinal muscles;Neuromuscular Disorders;2016-09
3. Lamin A/C mutations in dilated cardiomyopathy;Cardiology Journal;2014-08-29
4. Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease;PLoS ONE;2013-12-12
5. Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations;Muscle & Nerve;2013-06-28
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