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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