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Article

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis.

Clinica chimica acta; international journal of clinical chemistry - 24 Dec 2012

Chu Pei-Yi, Cheng Chih-Jen, Tseng Min-Hua, Yang Sung-Sen, Chen Hsiang-Cheng, Lin Shih-Hua

Abstract excerpt

BACKGROUND: A recent genome-wide association study of Thai patients with thyrotoxic periodic paralysis (TPP) identified a novel genetic variant rs623011 located in chromosome 17q24.3, which may potentially reduce the transcription of Kir2.1 and total Kir current. PURPOSE: The aim of this study was to evaluate whether this genetic variant was present in Chinese patients with TPP and sporadic periodic paralysis...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22910584
DOI: 10.1016/j.cca.2012.08.004

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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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