Title: | An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
Journal : | The Journal of general physiology, 149, 12 |
Authors: | Cannon SC, Author |
Material Type: | Article |
Publication Date: | 2017 |
Size: | p 1061 |
Languages: | English |
Keywords : | CACNA1S gene ; calcium channels ; familial hypokalemic periodic paralysis ; genetic mutations ; hypokalemia ; ion flux ; SCN4A gene ; skeletal muscle |
Abstract: |
Comment on:
Elevated resting H+ current in the R1239H type 1 hypokalaemic periodic paralysis mutated Ca2+ channel. [J Physiol. 2017] |
Pubmed / DOI : | DOI : 10.1085/jgp.201711923 / Pubmed : 29138267 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/29138267 |