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Updated: Jun 15, 2025

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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Loss of Methyltransferase and Hypomethylated m6A Sarcomere Transcripts Leading to Early-Onset Dilated Cardiomyopathy

Sophie Marie Hand1, Yi Zhao2, Donna Li1

  • 1Center for Cardiovascular Research, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH (S.M.H., D.L., S.B., J.Y., V.G., D.L., J.J.).

Circulation
|June 9, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
RNA metabolismdilated cardiomyopathyheart developmentm6A methyltransferasesarcomere

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