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About this Medicine article
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy by 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; R. Jongbloed; B. J. M. Smeets is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- 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; R. Jongbloed; B. J. M. Smeets
- Publisher
- Bohn Stafleu van Loghum; Springer-Verlag; Mediselect B.V.; Springer Science and Business Media LLC (ISSN 1568-5888)
- Published
- 2011
- Language
- EN
- Field
- Medicine (Health Sciences)