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Article

[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome].

Archives des maladies du coeur et des vaisseaux - 1 May 2007

Denjoy I, Lupoglazoff J-M, Villain E, Vaksmann G, Godart F, Lucet V, Leenhardt A, Guicheney P, Schwartz P

Abstract excerpt

UNLABELLED: Data on the Jervell and Lange-Nielsen syndrome (JLN), the long QT syndrome (LQTS) variant associated with deafness and caused by homozygous or compound heterozygous mutations on the KCNQ1 or on the KCNE1 genes encoding the IKs current, are still largely based on case reports. We analy...

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Source

Identifiers

PMID: 17646758

Genes

KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-17646758-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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