Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals

This publication has 121 references indexed in Scilit:

• A Glimpse Into Multigene Rare Variant Genetics: Triple Mutations in Hypertrophic Cardiomyopathy
  Journal of the American College of Cardiology, 2010
• Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation
  Journal of the American College of Cardiology, 2010
• Exome sequencing identifies the cause of a mendelian disorder
  Nature Genetics, 2009
• Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy
  Published by Elsevier ,2009
• Targeted capture and massively parallel sequencing of 12 human exomes
  Nature, 2009
• Common vs. rare allele hypotheses for complex diseases
  Published by Elsevier ,2009
• The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
  European Journal of Human Genetics, 2009
• Common and rare variants in multifactorial susceptibility to common diseases
  Nature Genetics, 2008
• Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
  Published by Elsevier ,2008
• Beyond Mendel: an evolving view of human genetic disease transmission
  Nature Reviews Genetics, 2002