Phospholamban Gene Mutations Are Not Associated with Hypertrophic Cardiomyopathy in a Northern Greek Population

By Kalemi Theodora   Efthimiadis Georgios   Zioutas Dimitrios   Lambropoulos Alexandros   Mitakidou Anastasia   Giannakoulas Georgios   Vassilikos Vassilios   Karvounis Haralambos   Kotsis Alexandros   Parharidis Georgios   Louridas Georgios  

Biochemical Genetics, Vol. 43, Iss. 11-12, 2005-12 ,pp. : 637-642

Springer Publishing Company

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Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene

By Gomes Aldrin V.   Potter James D.  

Molecular and Cellular Biochemistry, Vol. 263, Iss. 1, 2004-08 ,pp. : 99-114

Springer Publishing Company

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A low prevalence of MYH7 / MYBPC3 mutations among Familial Hypertrophic Cardiomyopathy patients in India

By Bashyam Murali  

Molecular and Cellular Biochemistry, Vol. 360, Iss. 1-2, 2012-01 ,pp. : 373-382

Springer Publishing Company

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A mouse model of familial hypertrophic cardiomyopathy caused by a -tropomyosin mutation

By Prabhakar R.   Petrashevskaya N.   Schwartz A.   Aronow B.   Boivin G.P.   Molkentin J.D.   Wieczorek D.F.  

Molecular and Cellular Biochemistry, Vol. 251, Iss. 1-2, 2003-09 ,pp. : 33-42

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Structural Analysis of the Titin Gene in Hypertrophic Cardiomyopathy: Identification of a Novel Disease Gene

By Satoh M.   Takahashi M.   Sakamoto T.   Hiroe M.   Marumo F.   Kimura A.  

Biochemical and Biophysical Research Communications, Vol. 262, Iss. 2, 1999-08 ,pp. : 411-417

Elsevier

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