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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Precision medicine approach to genetic cardiomyopathy

K Filonenko1, H A Katus1,2, B Meder3,4

  • 1Institute for Cardiomyopathies Heidelberg, University Heidelberg, Im Neuenheimer Feld 669, 69120, Heidelberg, Germany.

Herz
|June 28, 2017
PubMed

Keywords:
ArrhythmiaClustered regularly interspaced short palindromic repeatsGene repairGenetic testingGenome-wide association studyMutationsRisk assessmentSudden cardiac death

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