Genetic analysis and clinical features of familial hypokalemic periodic paralysis

Genetic analysis and clinical features of familial hypokalemic periodic paralysis

<p><strong>Background </strong>To investigate the gene mutation and clinical features of hypokalemic periodic paralysis (HypoPP) in a Han family.<strong> Methods </strong> Mutation analyses of<em> CACNA1S</em>, <em>SCN4A</em> and <em>KCNE...

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Bibliographic Details
Main Authors: Hui-li ZHANG, Yi-ming SUN, Min-ying ZHENG, Yu-ling ZHU, Ji-qing CAO, Yu ZHANG, Ya-qin LI, Lang-hui DENG, Cheng ZHANG
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2014-06-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Hypokalemic periodic paralysis
Genes
Mutation
Pedigree
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/971

Internet

http://www.cjcnn.org/index.php/cjcnn/article/view/971

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