Corrochano, Silvia <br/><br/>
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.  [electronic resource] 

 -  Brain : a journal of neurology  Dec 2014 
 - 3171-85 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awu292  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>AMP-Activated Protein Kinases--genetics<br/>Animals<br/>Channelopathies--genetics<br/>Humans<br/>Mice<br/>Mutation--genetics<br/>Myotonia--genetics<br/>Myotonic Disorders--genetics<br/>NAV1.4 Voltage-Gated Sodium Channel--genetics<br/>Paralyses, Familial Periodic--genetics<br/>Pedigree