Case report: SCN4A p.R1135H gene variant in combination with thyrotoxicosis causing hypokalemic periodic paralysis

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

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Case report: SCN4A p.R1135H gene variant in combination with thyrotoxicosis causing hypokalemic periodic paralysis https://t.co/rOWphsPlYJ https://t.co/dsXh1i2aAj

18 Jan 2023

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New Research: Case report: SCN4A p.R1135H gene variant in combination with thyrotoxicosis causing hypokalemic periodic paralysis: Hypokalemic periodic paralysis (HPP) is a heterogeneous group of diseases characterized by intermittent episodes… https://t.co

17 Jan 2023

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