A calcium channel mutant mouse model of hypokalemic periodic paralysis

Hypokalemic periodic paralysis (HypoPP) is a familial skeletal muscle disorder that presents with recurrent episodes of severe weakness lasting hours to days associated with reduced serum potassium (K(+)). HypoPP is genetically heterogeneous, with missense mutations of a calcium channel (Ca(V)1.1) o...

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Detaylı Bibliyografya
Asıl Yazarlar: Wu, Fenfen, Mi, Wentao, Hernández-Ochoa, Erick O., Burns, Dennis K., Fu, Yu, Gray, Hillery F., Struyk, Arie F., Schneider, Martin F., Cannon, Stephen C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 2012
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3533564/
https://ncbi.nlm.nih.gov/pubmed/23187123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI66091
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