Case report: A novel CACNA1S mutation associated with hypokalemic periodic paralysis

Overview of attention for article published in Frontiers in Neurology, September 2023

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New Research: Case report: A novel CACNA1S mutation associated with hypokalemic periodic paralysis: Background Hypokalemic periodic paralysis (HypoKPP) is a rare neuromuscular genetic disorder causing recurrent episodes of flaccid paralysis.… #Neurology h

29 Sep 2023

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