Related Experiment Video
Updated: Sep 2, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Congenital Muscular Dystrophy due to POMGNT1 Mutation Presenting as Cardioembolic Stroke
Mary Iype1, Omana Surendran Mithran2, Anitha Ayyappan3
1Department of Pediatric Neurology, Government Medical College, Thiruvananthapuram, Kerala, India.
Annals of Indian Academy of Neurology
|August 8, 2022
Abstract
No abstract available in PubMed .
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