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The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis
PURPOSE: Familial hypokalemic periodic paralysis (HOKPP) is an autosomal dominant channelopathy characterized by episodic attacks of muscle weakness and hypokalemia. Mutations in the calcium channel gene, CACNA1S, or the sodium channel gene, SCN4A, have been found to be responsible for HOKPP; howeve...
Tallennettuna:
| Julkaisussa: | Korean J Pediatr |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Korean Pediatric Society
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4219947/ https://ncbi.nlm.nih.gov/pubmed/25379045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2014.57.10.445 |
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