The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
Open Access
- 1 October 2003
- journal article
- Published by Oxford University Press (OUP) in European Heart Journal
- Vol. 24 (20) , 1848-1853
- https://doi.org/10.1016/s0195-668x(03)00466-4
Abstract
Aims Hypertrophic cardiomyopathy (HCM) is caused by mutations in genes that encode sarcomeric proteins. In this study we investigated the involvementKeywords
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