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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

✍ Scribed 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

Book ID: 113102731
Publisher: Bohn Stafleu van Loghum
Year: 2011
Tongue: English
Weight: 261 KB
Volume: 19
Category: Article
ISSN: 1568-5888
DOI: 10.1007/s12471-011-0135-z

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