The L450F [Corrected] 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

Lire sur PubMed
Neurogenetics. 2013-08-21; 14(3-4): 257-258
DOI: 10.1007/s10048-013-0370-0

Lire sur PubMed
1. Neurogenetics. 2013 Nov;14(3-4):257-8. doi: 10.1007/s10048-013-0370-0. Epub 2013
Aug 21.
The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada
syndrome closer together.
Duarri A(1), Nibbeling E, Fokkens MR, Meijer M, Boddeke E, Lagrange E, Stevanin
G, Brice A, Durr A, Verbeek DS.
Author information:
(1)Department of Genetics, University Medical Center Groningen, University of
Groningen, Groningen, The Netherlands.
Erratum in
Neurogenetics. 2015 Jul;16(3):243.
DOI: 10.1007/s10048-013-0370-0
PMID: 23963749 [Indexed for MEDLINE]