Skeletal Muscle Dihydropyridine-Sensitive Calcium Channel (CACNA1S) Gene Mutations in Chinese Patients with Hypokalemic Periodic Paralysis
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference34 articles.
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1. Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients;Orphanet Journal of Rare Diseases;2024-04-12
2. Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes;neurogenetics;2021-10-05
3. CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis;Clinical Case Reports;2020-07
4. PharmGKB summary: very important pharmacogene information for CACNA1S;Pharmacogenetics and Genomics;2020-02
5. Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis;Neurology;2016-03-02
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