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Bingshan Li, S. Leal (2008)
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Emily Burkett, R. Hershberger (2005)
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R. Hershberger, Sharie Parks, Jessica Kushner, Duanxiang Li, S. Ludwigsen, P. Jakobs, D. Nauman, D. Burgess, Julie Partain, M. Litt (2008)
Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated CardiomyopathyClinical and Translational Science, 1
Rare mutations in more than 20 genes have been suggested to cause dilated cardiomyopathy (DCM), but explain only a small percentage of cases, mainly in familial forms. We hypothesised that more common variants may also play a role in increasing genetic susceptibility to DCM, similar to that observed in other common complex disorders.
Annals of Human Genetics – Wiley
Published: Jan 1, 2010
Keywords: ; ; ;
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