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Updated: Aug 8, 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

Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred

Danielle E Dye1, Biagio Azzarelli, Hans H Goebel

  • 1Molecular Neurogenetics Laboratory, Centre for Medical Research, West Australian Institute for Medical Research, University of Western Australia M519, 'B' Block, Queen Elizabeth II Medical Centre, Nedlands, WA 6009, Australia.

Neuromuscular Disorders : NMD
|May 11, 2006
PubMed

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