Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes

Author:

Tadros Hanna J.,Life Chelsea S.,Garcia Gustavo,Pirozzi Elisa,Jones Edward G.,Datta Susmita,Parvatiyar Michelle S.,Chase P. Bryant,Allen Hugh D.,Kim Jeffrey J.,Pinto Jose R.,Landstrom Andrew P.

Funder

NIH

AHA SDG

Baylor College of Medicine Department of Pediatrics

Duke University School of Medicine

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference61 articles.

1. Cardiomyopathy: an overview;Wexler;Am. Fam. Physician,2009

2. Contemporary definitions and classification of the cardiomyopathies;Maron;Circulation.,2006

3. Cardiac troponin mutations and restrictive cardiomyopathy;Parvatiyar;J. Biomed. Biotechnol.,2010

4. Mutations in troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?;Willott;J. Mol. Cell. Cardiol.,2010

5. Regulation of contraction in striated muscle;Gordon;Physiol. Rev.,2000

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