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Original article
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish

Authors

  1. Dr A H Crosby, Medical Genetics Section, Clinical Developmental Sciences, St George’s University of London, Cranmer Terrace, London SW17 0RE, UK; acrosby{at}sgul.ac.uk
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Citation

Zahka K, Kalidas K, Simpson MA, et al
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish
Heart 2008;94:1326-1330.

Publication history

  • Accepted April 8, 2008
  • First published May 8, 2008.
Online issue publication 
March 15, 2016

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2008 BMJ Publishing Group and British Cardiac Society