![](/img/cover-not-exists.png)
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. P. Van Tintelen, J. D. H. Jongbloed, M. P. van den Berg, R. H. Lekanne Deprez, M. M. A. M. Mannens, N. Hofmann, M. Slegtenhorst, D. Dooijes, M. Michels, Y. Arens,Volume:
19
Language:
english
Pages:
8
DOI:
10.1007/s12471-011-0135-z
Date:
August, 2011
File:
PDF, 261 KB
english, 2011