Related Experiment Video

Updated: Jun 14, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

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

Published on: August 8, 2022

[Non-compaction cardiomyopathy: A rare echocardiographic diagnosis]

T Münkle1, H Kaufmann, M Keim

  • 1Hegau-Bodensee-Klinikum, I. Medizinische Klinik, Singen/Hohentwiel. thomas.muenkle@hbh-kliniken.de

Deutsche Medizinische Wochenschrift (1946)
|March 25, 2010
PubMed
Abstract

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