Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy

By Geier Christian   Gehmlich Katja   Ehler Elisabeth   Hassfeld Sabine   Perrot Andreas   Hayess Katrin   Cardim Nuno   Wenzel Katrin   Erdmann Bettina   Krackhardt Florian   Posch Maximilian G.   Bublak Angelika   Ngele Herbert   Scheffold Thomas   Dietz Rainer   Chien Kenneth R.   Spuler Simone   Frst Dieter O.   Nrnberg Peter   zcelik Cemil  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2753-2765

Oxford University Press

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Mutations in the γ 2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

By Blair E.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1215-1220

Oxford University Press

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Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

By Jaksch Michaela  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 795-801

Oxford University Press

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Phenotypic diversity in hypertrophic cardiomyopathy

By Arad M.   Seidman J.G.   Seidman C.E.  

Human Molecular Genetics, Vol. 11, Iss. 20, 2002-10 ,pp. : 2499-2506

Oxford University Press

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Point Mutations in Human GLI3 Cause Greig Syndrome

By Wild Anja   Kalff-Suske Martha   Vortkamp Andrea   Bornholdt Dorothea   Kônig Rainer   Grzeschik Karl-Heinz  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1979-1984

Oxford University Press

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