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Updated: Dec 24, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in
Colin J Mahoney1, Thanuja Dharmadasa1, William Huynh1
1Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
Muscle & Nerve
|April 10, 2020
Abstract
No abstract available in PubMed .
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