We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.AuthorsKe T; Gomez CR; Mateus HE; Castano JA; Wang QKPublicationJournal of human genetics, 2009, Vol 54, Issue 11, p660ISSN1435-232xPublication typearticleDOI10.1038/jhg.2009.92