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Updated: Aug 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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Erratum: Hypertrophic cardiomyopathy: Mutations to mechanisms to therapies

Frontiers Production Office1

  • 1Frontiers Media SA, Lausanne, Switzerland.

Frontiers in Physiology
|December 29, 2022
PubMed

Insights

This study corrects a previous article DOI. The corrected DOI ensures accurate citation and retrieval of the research findings for better scientific communication.

Area of Science:

  • Physiology
  • Scientific Publishing

Context:

  • Correction of a previously published article DOI.
  • Ensuring accurate citation and retrieval of scientific literature.

Purpose:

  • To provide the correct Digital Object Identifier (DOI) for the article.
  • To rectify errors in the article's metadata.

Summary:

  • The article DOI has been corrected to 10.3389/fphys.2022.975076.
  • This correction facilitates proper referencing and access to the research.

Impact:

  • Improved accuracy in scientific record-keeping.
  • Enhanced discoverability and citation of the research article.

Keywords:
hypertrophic cardiomyopathymavacamtenmyosinomecamtiv mercarbilsuper relaxed state

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