A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II-linker

Translated title of the contribution: A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II-linker

X.H.T. Wehrens, T. Rossenbacker, R.J. Jongbloed, M. Gewillig, H. Heidbuchel, P.A.F.M. Doevendans, M.A. Vos, H.J.J. Wellens, R.S. Kass

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionA novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II-linker
Original languageUndefined/Unknown
Pages (from-to)552
Number of pages1
JournalHuman Mutation
Volume21
Issue number5
Publication statusPublished - 2003

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde(GENK)
  • Algemeen onderzoek
  • Other medical specialities

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