An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis |
Journal of General Physiology | Rockefeller University Press Skip to Main Content …

An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis
An atypical Ca V 1.1 mutation reveals a common mechanism for hypokalemic periodic …

An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic
paralysis - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI …

Hypokalemic periodic paralysis (HypoKPP) is a rare, dominantly inherited disorder of
muscle that is characterized by recurrent and prolonged episodes of severe weakness …

An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic paralysis.
- Abstract - Europe PMC Sign in | Create an account https://orcid.org Europe PMC Menu About …

An atypical CaV1.1 mutation reveals a common mechanism for hypokalemic periodic
paralysis Page 1 Commentary The Rockefeller University Press J. Gen. Physiol. 2017 Vol …