Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy.

Translated title of the contribution: Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy.

R.J. Jongbloed, C.L. Marcelis, P.A.F.M. Doevendans, J.M. Schmeitz-Mulkens, W.G. van Dockum, J.P. Geraedts, H.J. Smeets

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contributionVariable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy.
Original languageUndefined/Unknown
Pages (from-to)981-986
Number of pages6
JournalJournal of the American College of Cardiology
Volume41
Publication statusPublished - 2003

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde(GENK)
  • Bescherming en bevordering van de menselijke gezondheid
  • Other medical specialities

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