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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...

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Detalhes bibliográficos
Publicado no:Korean J Pediatr
Main Authors: Kim, June-Bum, Kim, Sung-Jo, Kang, Sun-Yang, Yi, Jin Woong, Kim, Seung-Min
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Pediatric Society 2014
Assuntos:
Acesso em linha: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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