Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Translated title of the contribution: Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

M.B. Rook, C. Bezzina, W.A. Groenewegen, L.J. Herfst, A.C. van der Wal, J. Lam, H.J. Jongsma, A.A.M. Wilde, M.M.A.M. Mannens

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionCompound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.
Original languageUndefined/Unknown
Pages (from-to)159-168
Number of pages10
JournalCirculation Research
Volume92
Issue number2
Publication statusPublished - 2002

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde (GENK)
  • Geneeskunde(GENK)
  • Bescherming en bevordering van de menselijke gezondheid
  • Other medical specialities

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