A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference32 articles.
1. Phenotype variation and newcomers in ion channel disorders
2. Identification of a mutation in the gene causing hyperkalemic periodic paralysis
3. A Met-to-Val mutation in the skeletal muscle Na+ channel α-subunit in hyperkalaemic periodic paralysis
4. Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel
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3. Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses;Scientific Reports;2018-02-01
4. Sudden Cardiac Death and Disorders of the QT Interval: Anesthetic Implications and Focus on Perioperative Management;Journal of Cardiothoracic and Vascular Anesthesia;2015-12
5. Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis;Brain;2014-10-20
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