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 journal › Article › Academic › peer-review
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