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Article

Expression patterns of two potassium channel genes in skeletal muscle cells of patients with familial hypokalemic periodic paralysis.

Neurology India - 1 Jan 2000

Kim June-Bum, Lee Gyung-Min, Kim Sung-Jo, Yoon Dong-Ho, Lee Young-Hyuk

Abstract excerpt

BACKGROUND: Familial hypokalemic periodic paralysis is an autosomal-dominant disorder characterized by episodic attacks of muscle weakness with hypokalemia. The combination of sarcolemmal depolarization and hypokalemia has been attributed to abnormalities of the potassium conductance governing the membrane potential; however, the molecular mechanism that causes hypokalemia has not yet been determined. AIM: To...

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Source

Identifiers

PMID: 21891927
DOI: 10.4103/0028-3886.84331

Genes

KCNQ3
KCNQ5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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