Arvelige hjertesygdomme forårsaget af natriumkanalmutationer

Jacob Tfelt-Hansen, Søren-Peter Olesen, Jesper Hastrup Svendsen, Thomas Jespersen

    Abstract

    Contraction of the heart is achieved through a delicately regulated conduction of electrical impulses. A pivotal element in the impulse propagation is the depolarising sodium current responsible for the initial depolarisation of the cardiomyocytes. Recent research has shown that mutations in the gene encoding the cardiac sodium channel (SCN5A) is associated with both rare forms of ventricular arrhythmia, and with the most frequent form of arrhythmia, atrial fibrillation.

    Bidragets oversatte titelInherited cardiac diseases caused by Nav1.5 sodium channel mutations
    OriginalsprogDansk
    TidsskriftUgeskrift for Laeger
    Vol/bind171
    Udgave nummer15
    Sider (fra-til)1261-5
    Antal sider5
    ISSN0041-5782
    StatusUdgivet - 6 apr. 2009

    Emneord

    • Atrial Fibrillation
    • Brugada Syndrome
    • Heart Conduction System
    • Humans
    • Long QT Syndrome
    • Muscle Proteins
    • Mutation
    • NAV1.5 Voltage-Gated Sodium Channel
    • Sodium Channels

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