Recurrent and founder mutations in the Netherlands: the cardiac phenotype of founder mutations p.S13F and p.N342D

K. Y. van Spaendonck-Zwarts*, A. J. van der Kooi, M. P. van den Berg, E. F. Ippel, L. G. Boven, W. -C. Yee, A. van den Wijngaard, E. Brusse, J. E. Hoogendijk, P. A. Doevendans, M. de Visser, J. D. H. Jongbloed, J. P. van Tintelen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)219-228
JournalNetherlands Heart Journal
Issue number5
Publication statusPublished - May 2012


  • Desmin
  • Genetics
  • Founder mutation
  • Cardiomyopathy
  • Cardiac conduction disease

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