The val606met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age

Ole Havndrup, Henning Bundgaard, Paal S. Andersen, Lars A. Larsen, Jens Vuust, Keld Kjeldsen, Michael Christiansen*

*Corresponding author af dette arbejde

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review

    Abstrakt

    A study of published families disclosed that the Val606Met mutation in β-myosin heavy chain carries a high risk of sudden death at a young age. The association of a specific mutation with a certain phenotype should be based on a large number of families to avoid sampling bias.

    OriginalsprogEngelsk
    Sider (fra-til)1315-1317
    Antal sider3
    TidsskriftAmerican Journal of Cardiology
    Vol/bind87
    Udgave nummer11
    DOI
    StatusUdgivet - 1 jun. 2001

    Fingeraftryk

    Udforsk hvilke forskningsemner 'The val<sup>606</sup>met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age' indeholder.

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