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  • Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

    Published in:
    Human Mutation, 2006, v. 27, n. 9, p. 914, doi. 10.1002/humu.20350
    By:
    • Suls, Arvid;
    • Claeys, Kristl G.;
    • Goossens, Dirk;
    • Harding, Boris;
    • Luijk, Rob Van;
    • Scheers, Stefaan;
    • Deprez, Liesbet;
    • Audenaert, Dominique;
    • Dyck, Tine Van;
    • Beeckmans, Sabine;
    • Smouts, Iris;
    • Ceulemans, Berten;
    • Lagae, Lieven;
    • Buyse, Gunnar;
    • Barisic, Nina;
    • Misson, Jean-Paul;
    • Wauters, Jan;
    • Del-Favero, Jurgen;
    • De Jonghe, Peter;
    • Claes, Lieve R.F.
    Publication type:
    Article