Skip to search formSkip to main contentSkip to account menu

Hypokalemic periodic paralysis type 1

Known as: HYPOKALEMIC PERIODIC PARALYSIS, HOKPP1, HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1 
National Institutes of Health

Related topics

Related topics

1 relation
Autosomal dominant inheritance

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Gating of the HypoPP-1 mutations: I. Mutant-specific effects and cooperativity
Hypokalemic periodic paralysis type 1 (HypoPP-1) is a hereditary muscular disorder caused by point mutations in the gene encoding… 
2007
2007
Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644
L-type calcium-channel mutations causing hypokalemic periodic paralysis type 1 (HypoPP-1) have pronounced “loss-of-function… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)