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.
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APA
Rezkalla, N., Imam, K., Marti, M., Ip, K., Mashhadian, A., & Liu, A. (2020). CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis. Clinical Case Reports, 8(10), 1962–1964. https://doi.org/10.1002/ccr3.3054
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