A carregar...
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...
Na minha lista:
| Publicado no: | Korean J Pediatr |
|---|---|
| Main Authors: | , , , , |
| 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|