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Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy

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Main Authors: Friedrich, Felix (Author) , Wilding, Brendan R. (Author) , Reischmann, Silke (Author) , Crocini, Claudia (Author) , Lang, Patrick (Author) , Charron, Philippe (Author) , Müller, Oliver J. (Author) , McGrath, Meagan J. (Author) , Vollert, Ingra (Author) , Hansen, Arne (Author) , Linke, Wolfgang A. (Author) , Hengstenberg, Christian (Author) , Bonne, Gisèle (Author) , Morner, Stellan (Author) , Wichter, Thomas (Author) , Madeira, Hugo (Author) , Arbustini, Eloisa (Author) , Eschenhagen, Thomas (Author) , Mitchell, Christina A. (Author) , Isnard, Richard (Author) , Carrier, Lucie (Author)
Format: Article (Journal)
Language:English
Published: 2012
In: Human molecular genetics
Year: 2012, Volume: 21, Issue: 14, Pages: 3237-3254
ISSN:0964-6906
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Author Notes:Felix W. Friedrich, Brendan R. Wilding, Silke Reischmann, Claudia Crocini, Patrick Lang, Philippe Charron, Oliver J. Müller, Meagan J. McGrath, Ingra Vollert, Arne Hansen, Wolfgang A. Linke, Christian Hengstenberg, Gisèle Bonne, Stellan Morner, Thomas Wichter, Hugo Madeira, Eloisa Arbustini, Thomas Eschenhagen, Christina A. Mitchell, Richard Isnard, Lucie Carrier
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ISSN:0964-6906

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