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CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis.

Abstract
It has long been believed that the patients with thyrotoxic hypokalemic periodic paralysis (THPP) may harbor genetic mutations commonly found in familial hypokalemic periodic paralysis. Despite extensive testing, such a mutation has escaped detection until now.
AuthorsNader Rezkalla, Kamran Imam, Miriam Marti, Karen Ip, Ardavan Mashhadian, Antonio Liu
JournalClinical case reports (Clin Case Rep) Vol. 8 Issue 10 Pg. 1962-1964 (Oct 2020) ISSN: 2050-0904 [Print] England
PMID33088529 (Publication Type: Case Reports)
Copyright© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

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