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*

*Corresponding author for this work

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

12 Citations (Scopus)
Original languageEnglish
Pages (from-to)257-258
Number of pages2
JournalNeurogenetics
Volume14
Issue number3-4
DOIs
Publication statusPublished - Nov-2013

Keywords

  • Adult
  • Brugada Syndrome
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Shal Potassium Channels
  • Spinocerebellar Ataxias

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