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Article

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

Clinical endocrinology - 1 Jul 2004

Tang Nelson L S, Chow C C, Ko Gary T C, Tai Morris H L, Kwok Rachel, Yao X Q, Cockram Clive S

Abstract excerpt

OBJECTIVES: Mutation in KCNE3 gene (Isk-related family potassium voltage-gated channel member 3 gene) was recently associated with the aetiology of thyrotoxic periodic paralysis (TPP). We studied 79 Chinese TPP patients by DNA sequencing of the entire coding sequence of KCNE3 to determine if this...

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Identifiers

PMID: 15212652
DOI: 10.1111/j.1365-2265.2004.02079.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15212652-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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