Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.
Corrochano, Silvia
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
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2156
10.1093/brain/awu292 doi
AMP-Activated Protein Kinases--genetics
Animals
Channelopathies--genetics
Humans
Mice
Mutation--genetics
Myotonia--genetics
Myotonic Disorders--genetics
NAV1.4 Voltage-Gated Sodium Channel--genetics
Paralyses, Familial Periodic--genetics
Pedigree
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
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2156
10.1093/brain/awu292 doi
AMP-Activated Protein Kinases--genetics
Animals
Channelopathies--genetics
Humans
Mice
Mutation--genetics
Myotonia--genetics
Myotonic Disorders--genetics
NAV1.4 Voltage-Gated Sodium Channel--genetics
Paralyses, Familial Periodic--genetics
Pedigree