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Updated: Jun 24, 2026

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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A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy

B C Mobley1, G M Enns, L-J Wong

  • 1Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA. bretmobley@gmail.com

Clinical Neuropathology
|April 10, 2009
PubMed

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