Mechanisms underlying a life-threatening skeletal muscle Na+channel disorder
Author:
Publisher
Wiley
Subject
Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/jphysiol.2011.207977/fullpdf
Reference36 articles.
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3. A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation;Bouhours;J Physiol,2005
4. Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans;Bouhours;J Physiol,2004
5. Immunoaffinity isolation of Na+ channels from rat skeletal muscle. Analysis of subunits;Casadei;J Biol Chem,1986
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