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Autor:
William J. McKenna, Judith Montag, Bernhard Brenner, Snigdha Tripathi, Edgar Becker, Francisco Navarro-López, Anna-Lena Weber, Imke Schulte, Andreas Perrot, Özcelik Cemil, Bianka Borchert, Karl-Josef Osterziel, Antonio Francino, Theresia Kraft
Publikováno v:
ResearcherID
Familial Hypertrophic Cardiomyopathy (FHC) is an autosomal dominant disease of the heart. The severity of the disease ranges from mild cases to sudden cardiac death or progression to heart failure. FHC is mostly caused by mutations in genes encoding
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