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Hypokalemic periodic paralysis type 1
Known as:
HYPOKALEMIC PERIODIC PARALYSIS
, HOKPP1
, HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1
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National Institutes of Health
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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
Alexey Kuzmenkin
,
C. Hang
,
Elza Kuzmenkina
,
K. Jurkat-Rott
Pflügers Archiv: European Journal of Physiology
2007
Corpus ID: 7326985
Hypokalemic periodic paralysis type 1 (HypoPP-1) is a hereditary muscular disorder caused by point mutations in the gene encoding…
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2007
2007
Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644
Alexey Kuzmenkin
,
C. Hang
,
Elza Kuzmenkina
,
K. Jurkat-Rott
Pflügers Archiv: European Journal of Physiology
2007
Corpus ID: 26714103
L-type calcium-channel mutations causing hypokalemic periodic paralysis type 1 (HypoPP-1) have pronounced “loss-of-function…
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