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Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling
  1. Correspondence to:
 Associate Professor Christopher Semsarian
 Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Locked Bag 6, Newtown, NSW 2042, Australia; c.semsariancentenary.usyd.edu.au
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Citation

Ingles J, Doolan A, Chiu C, et al
Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

Publication history

  • Received April 11, 2005
  • Accepted May 13, 2005
  • Revised May 11, 2005
  • First published September 30, 2005.
Online issue publication 
November 02, 2016

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