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

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 journal › Article › Academic › peer-review

Translated title of the contribution	Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy
Original language	Undefined/Unknown
Pages (from-to)	478-485
Number of pages	8
Journal	Netherlands Heart Journal
Volume	18
Issue number	10
Publication status	Published - 2010

Cite this

Otten, E., Lekanne Dit Deprez, R. H., Weiss, M. M., van Slegtenhorst, M., Joosten, M., van der Smagt, J. J., de Jonge, N., Kerstjens-Frederikse, W. S., Roofthooft, M. T., Balk, A. H., van den Berg, M. P., Ruiter, J. S., & van Tintelen, J. P. (2010). Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy. Netherlands Heart Journal, 18(10), 478-485.

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

author = "E. Otten and \{Lekanne Dit Deprez\}, R.H. and M.M. Weiss and \{van Slegtenhorst\}, M. and M. Joosten and \{van der Smagt\}, J.J. and \{de Jonge\}, N. and W.S. Kerstjens-Frederikse and M.T. Roofthooft and A.H. Balk and \{van den Berg\}, M.P. and J.S. Ruiter and \{van Tintelen\}, J.P.",

year = "2010",

language = "Undefined/Unknown",

volume = "18",

pages = "478--485",

journal = "Netherlands Heart Journal",

issn = "1568-5888",

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Otten, E, Lekanne Dit Deprez, RH, Weiss, MM, van Slegtenhorst, M, Joosten, M, van der Smagt, JJ, de Jonge, N, Kerstjens-Frederikse, WS, Roofthooft, MT, Balk, AH, van den Berg, MP, Ruiter, JS & van Tintelen, JP 2010, 'Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy', Netherlands Heart Journal, vol. 18, no. 10, pp. 478-485.

TY - JOUR

T1 - Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy

AU - Otten, E.

AU - Lekanne Dit Deprez, R.H.

AU - Weiss, M.M.

AU - van Slegtenhorst, M.

AU - Joosten, M.

AU - van der Smagt, J.J.

AU - de Jonge, N.

AU - Kerstjens-Frederikse, W.S.

AU - Roofthooft, M.T.

AU - Balk, A.H.

AU - van den Berg, M.P.

AU - Ruiter, J.S.

AU - van Tintelen, J.P.

PY - 2010

Y1 - 2010

M3 - Article

SN - 1568-5888

VL - 18

SP - 478

EP - 485

JO - Netherlands Heart Journal

JF - Netherlands Heart Journal

IS - 10

ER -