Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

A. van den Wijngaard, P. Volders, J. Peter van Tintelen, Jan D. H. Jongbloed, M. P. van den Berg, Ronald H. Lekanne Deprez, Marcel M. A. M. Mannens, N. Hofmann, Marjon van Slegtenhorst, Dennis Dooijes, Michelle Michels, Y. Arens, R. Jongbloed, B. J. M. Smeets

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)344-351
JournalNetherlands Heart Journal
Volume19
Issue number7-8
DOIs
Publication statusPublished - Aug 2011

Keywords

  • TNNI3
  • Founder
  • HCM
  • RCM
  • DCM

Cite this

van den Wijngaard, A., Volders, P., van Tintelen, J. P., Jongbloed, J. D. H., van den Berg, M. P., Deprez, R. H. L., Mannens, M. M. A. M., Hofmann, N., van Slegtenhorst, M., Dooijes, D., Michels, M., Arens, Y., Jongbloed, R., & Smeets, B. J. M. (2011). Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy. Netherlands Heart Journal, 19(7-8), 344-351. https://doi.org/10.1007/s12471-011-0135-z