Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

Hypertrophic cardiomyopathy (HCM) is a frequent genetic cardiac disease and the most common cause of sudden cardiac death in young individuals. Most of the currently known HCM disease genes encode sarcomeric proteins. Previous studies have shown an association between CSRP3 missense mutations and ei...

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Bibliographic Details
Main Authors: Geier, C, Gehmlich, K, Ehler, E, Hassfeld, S, Perrot, A, Hayess, K, Cardim, N, Wenzel, K, Erdmann, B, Krackhardt, F, Posch, MG, Osterziel, K, Bublak, A, Nägele, H, Scheffold, T, Dietz, R, Chien, K, Spuler, S, Fürst, DO, Nürnberg, P, Ozcelik, C
Format: Journal article
Language:English
Published: 2008