(2009). Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
Chicago Style (17th ed.) CitationNovel CACNA1S Mutation Causes Autosomal Dominant Hypokalemic Periodic Paralysis in a South American Family. 2009.
MLA (8th ed.) CitationNovel CACNA1S Mutation Causes Autosomal Dominant Hypokalemic Periodic Paralysis in a South American Family. 2009.
Warning: These citations may not always be 100% accurate.