Hyperkalemic periodic paralysis with cardiac dysrhythmia: A novel sodium channel mutation?
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference16 articles.
1. Hyperkalemic periodic paralysis: Rapid molecular diagnosis and relationship of genotype to phenotype in 12 families
2. Genotype-Phenotype Correlations in Human Skeletal Muscle Sodium Channel Diseases
3. Duchenne-Becker Muscular Dystrophy and the Nondystrophic Myotonias
4. Functional expression of sodium channel mutations identified in families with periodic paralysis
5. Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker.
Cited by 16 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. SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies;European Journal of Human Genetics;2015-06-03
2. Skeletal muscle Na+ channel disorders;Frontiers in Pharmacology;2011
3. Mutations of Sodium Channel α-Subunit Genes in Chinese Patients with Normokalemic Periodic Paralysis;Cellular and Molecular Neurobiology;2007-11-29
4. Periodic paralysis;Handbook of Clinical Neurology;2007
5. Familial Periodic Paralysis and Charcot-Marie-Tooth Disease in a 7-Generation Family;Archives of Neurology;2005-01-01
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