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Rigshospitalet - a part of Copenhagen University Hospital
Published

KCNE1 G38S polymorphism is not the cause of long QT syndrome

Research output: Contribution to journalJournal articleResearchpeer-review

  1. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Gain-of-function mutation in the voltage-gated potassium channel gene KCNQ1 and glucose-stimulated hypoinsulinemia - case report

    Research output: Contribution to journalJournal articleResearchpeer-review

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Original languageEnglish
JournalJournal of Electrocardiology
Volume49
Issue number2
Pages (from-to)249-50
ISSN0022-0736
DOIs
Publication statusPublished - 12 Dec 2016

ID: 46230143