The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis
PurposeFamilial 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; however,...
Sábháilte in:
| Príomhchruthaitheoirí: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Korean Pediatric Society
2014-10-01
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| Sraith: | Korean Journal of Pediatrics |
| Ábhair: | |
| Rochtain ar líne: | http://kjp.or.kr/upload/pdf/kjped-57-445.pdf |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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