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Article

Phenotypic analysis of vertigo 2 Jackson mice with a Kcnq1 potassium channel mutation.

Experimental animals - 1 Jul 2007

Takagi Takeshi, Nishio Hajime, Yagi Takeo, Kuwahara Masayoshi, Tsubone Hirokazu, Tanigawa Nobuhiko, Suzuki Koichi

Abstract excerpt

The KCNQ1 gene encodes a voltage-dependent potassium ion channel, and mutations in this gene are the most common cause of congenital long QT syndrome (LQTS). In the present study, we investigated the various phenotypic characteristics of vertigo 2 Jackson (C3H/HeJCrl-Kcnq1(vtg-2J)/J) mice with a...

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Source

Identifiers

PMID: 17660684
DOI: 10.1538/expanim.56.295

Genes

KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17660684-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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