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

Title
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
Authors
Keywords
-
Journal
Netherlands Heart Journal
Volume 19, Issue 7-8, Pages 344-351
Publisher
Springer Nature
Online
2011-05-01
DOI
10.1007/s12471-011-0135-z

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