De novo SCN1A mutations ara a major cause of severe myoclonic epilepsy of infancy

Authors
Publication date
1 January 2003
Publisher

Abstract

Abstract is not available.

    Similar works

    Full text

    thumbnail-image

    Available Versions

    Institutional Repository Universiteit Antwerpen

    redirect
    oaic:irua:45550
    Last time updated on 18/12/2017