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Updated: Jul 23, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

作者纠正:BHMT多态性和在中国患者中对PTE的敏感性

W-H Zhang¹, S-M Zhao, J-F Guo

¹Department of Cardiovascular Medicine, the First Hospital of Jilin University, Changchun, Jilin Province, China.

European review for medical and pharmacological sciences

|July 17, 2023

概括

这项研究的纠正更新了以前在网上发布的研究资金信息. 吉林省科技部支持了这项工作.

科学领域:

药理学和医学科学药理学和医学科学

背景情况:

"欧洲医学和药理科学评论"上一篇文章需要纠正.
修正涉及到发表文章的资金确认部分.

研究的目的:

修改原始研究的资金信息.
确保研究支持的准确分配.

主要方法:

作者在最初的资金声明中发现了一个遗漏.
资金部分在发布后进行了更新,以反映正确的支持来源.

主要成果:

这项研究得到了吉林省科技部研究计划的支持.
具体的赠款号码是 20190201011J. 具体的赠款号码是 20190201011J.

结论:

修正确保了研究资金的透明度和准确报告.
这项修正案澄清了科学研究的财政支持.

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