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Impaired calcium handling and mitochondrial metabolic dysfunction as early markers of hypertrophic cardiomyopathy

  • Published:2019-04 Issue: Volume:665 Page:166-174
  • ISSN:0003-9861
  • Container-title:Archives of Biochemistry and Biophysics
  • language:en
  • Short-container-title:Archives of Biochemistry and Biophysics

Author:

Viola Helena M.,Hool Livia C.

Funder

National Heart Foundation of Australia Research Fellow

National Health and Medical Research Council of Australia

Raine Medical Research Foundation

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference106 articles.

1. Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy;Roma-Rodrigues;Appl. Clin. Genet.,2014

2. Genetics of hypertrophic cardiomyopathy: a review of current state;Sabater-Molina;Clin. Genet.,2018

3. New perspectives on the prevalence of hypertrophic cardiomyopathy;Semsarian;J. Am. Coll. Cardiol.,2015

4. Contemporary insights and strategies for risk stratification and prevention of sudden death in hypertrophic cardiomyopathy;Maron;Circulation,2010

5. Clinical and mechanistic insights into the genetics of cardiomyopathy;Burke;J. Am. Coll. Cardiol.,2016
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