Lamin A/C mutation affecting primarily the right side of the heart

<em>LMNA</em> mutations are amongst the most important causes of familial dilated cardiomyopathy. The most important cause of arrhythmogenic right ventricular cardiomyopathy (ARVC) is desmosomal pathology. The aim of the study was to elucidate the role of <em>LMNA</em> mutati...

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Main Authors: Laura Ollila, Johanna Kuusisto, Keijo Peuhkurinen, Satu Kärkkäinen, Petri Tuomainen, Maija Kaartinen, Olayinka Raheem, Bjarne Udd, Jarkko Magga, Janne Rapola, Annukka M. Lahtinen, Eero Lehtonen, Miia Holmström, Sari Kivistö, Elisabeth Widén, Markku Saksa, Tiina Heliö
Format: Article
Language:English
Published: MDPI AG 2013-04-01
Series:Cardiogenetics
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Online Access:http://www.pagepressjournals.org/index.php/cardiogen/article/view/673