Related Experiment Video
Updated: Mar 24, 2026

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Meyer dysplasia: a diagnosis to consider
Ana Teresa Maria1, Raquel Firme1, Pedro Magro2
1Department of Paediatrics, Hospital de Cascais, Cascais, Portugal.
BMJ Case Reports
|March 11, 2016
Summary
No abstract available in PubMed .
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