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Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy

Translated title of the contribution: Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy
  • E. Otten
  • , R.H. Lekanne Dit Deprez
  • , M.M. Weiss
  • , M. van Slegtenhorst
  • , M. Joosten
  • , J.J. van der Smagt
  • , N. de Jonge
  • , W.S. Kerstjens-Frederikse
  • , M.T. Roofthooft
  • , A.H. Balk
  • , M.P. van den Berg
  • , J.S. Ruiter
  • , J.P. van Tintelen

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionRecurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy
Original languageUndefined/Unknown
Pages (from-to)478-485
Number of pages8
JournalNetherlands Heart Journal
Volume18
Issue number10
Publication statusPublished - 2010

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