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Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy

Andreas Brodehl1, Raechel A Ferrier2, Sara J Hamilton3

  • 1Department of Cardiac Sciences, Libin Cardiovascular Institute of Alberta, University of Calgary, Calgary, Alberta, Canada.

Human Mutation
|December 16, 2015
PubMed

Keywords:
FLNCexome sequencingfilamin-Cheart failurerestrictive cardiomyopathy

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