论文信息 - Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy - 字舞流文

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

M. P. van den Berg | P. Volders | R. L. Lekanne Deprez | M. Mannens | R. Jongbloed | J. P. van Tintelen | J. P. Tintelen | J. Jongbloed | M. Michels | M. Mannens | R. H. L. Deprez | A. van den Wijngaard | M. Slegtenhorst | A. Wijngaard | D. Dooijes | Y. Arens | R. Jongbloed | Y. Arens | B. Smeets | N. Hofmann | M. V. Slegtenhorst | M. P. Berg