The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

Anna Duarri, Esther Nibbeling, Michiel R. Fokkens, Michel Meijer, Erik Boddeke, Emmeline Lagrange, Giovanni Stevanin, Alexis Brice, Alexandra Durr, Dineke S. Verbeek
Neurogenetics. 2013-08-21; 14(3-4): 257-258
DOI: 10.1007/s10048-013-0370-0

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