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

van den Wijngaard, A, Volders, P, Tintelen, JP, Jongbloed, JDH, Lambregtse - van den Berg, Mijke, Deprez, RHL, Mannens, MMAM, Hofmann, N, van Slegtenhorst, M, Dooijes, D, Michels, Michelle, Arens, Y, Jongbloed, R, Smeets, BJM
Veröffentlicht in: van den Wijngaard , A , Volders , P , Tintelen , JP , Jongbloed , JDH , Lambregtse - van den Berg , M , Deprez , RHL , Mannens , MMAM , Hofmann , N , van Slegtenhorst , M , Dooijes , D , Michels , M , Arens , Y , Jongbloed , R & Smeets , BJM 2011 , ' Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy ' , Netherlands Heart Journal , vol. 19 , no. 7-8 , pp. 344-351 . https://doi.org/10.1007/s12471-011-0135-z;
2011

Originalkatalog | Verfügbarkeit prüfen

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

Wijngaard, A. (Arthur) van den, Volders, P.G.A. (Paul), Tintelen, J.P. (Peter) van, Jongbloed, J.D.H. (Jan), Berg, M.P. (Maarten) van den, Lekanne Deprez, R.H., Mannens, M.M.A.M. (Marcel), Hofmann, N., Slegtenhorst, M.A. (Marjon) van, Dooijes, D. (Dennis), Michels, M. (Michelle), Arens, Y.H.J.M. (Yvonne), Smeets, B.J.M.
2011