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Article

Mutation screening in Chinese hypokalemic periodic paralysis patients.

Molecular genetics and metabolism - 1 Apr 2006

Wang Weiqing, Jiang Lei, Ye Lei, Zhu Na, Su Tingwei, Guan Liqing, Li Xiaoying, Ning Guang

Abstract excerpt

Thyrotoxic periodic paralysis (TPP), familial periodic paralysis (FPP), and sporadic periodic paralysis (SPP) are the most common causes of hypokalemic periodic paralysis (hypoKPP). The patients present with similar clinical features characterized by episodic attacks of muscle weakness and a decrease in blood potassium. Mutations in the gene encoding the voltage-sensor coding regions of the skeletal muscle sodium...

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Identifiers

PMID: 16386935
DOI: 10.1016/j.ymgme.2005.10.020

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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