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The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
Authors: Alders, M.; Jongbloed, R.; Deelen, W.; van den Wijngaard, A.; Doevendans, P.; Ten Cate, F.; Regitz-Zagrosek, V.; Vosberg, H. P.; van Langen, I.; Wilde, A.; Dooijes, D.; Mannens, M.
Date of Publication (YYYY-MM-DD): 2003-10
Title of Journal: European Heart Journal
Volume: 24
Issue / Number: 20
Start Page: 1848
End Page: 1853
Document Type: Article
ID: 199036.0
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