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

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)219-228
JournalNetherlands Heart Journal
Volume20
Issue number5
DOIs
Publication statusPublished - May 2012

Keywords

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

Cite this

van Spaendonck-Zwarts, K. Y., van der Kooi, A. J., van den Berg, M. P., Ippel, E. F., Boven, L. G., Yee, W. -C., van den Wijngaard, A., Brusse, E., Hoogendijk, J. E., Doevendans, P. A., de Visser, M., Jongbloed, J. D. H., & van Tintelen, J. P. (2012). Recurrent and founder mutations in the Netherlands: the cardiac phenotype of founder mutations p.S13F and p.N342D. Netherlands Heart Journal, 20(5), 219-228. https://doi.org/10.1007/s12471-011-0233-y