相关实验视频

Updated: Jul 1, 2025

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells

Published on: July 29, 2016

对"扩大RBCK1-关联多糖体肌肉病变1型的表型"的纠正

Manuel Pühringer¹, Astrid Eisenkölbl¹, Gudrun Gröppel^1,2

¹Department of Paediatrics and Adolescent Medicine, Kepler University Hospital, Linz, Austria.

Molecular genetics and metabolism reports

|March 12, 2024

概括

这项研究纠正了先前发表的一篇文章DOI. 校正确保了准确的引用,用于该领域的未来研究.

科学领域:

遗传学和基因组学遗传学和基因组学
分子生物学分子生物学

背景情况:

准确的科学文献对于研究完整性至关重要.
适当的引用和DOI引用是学术交流的基础.

研究的目的:

为特定的物品提供纠正DOI.
确保科学记录是准确和可检索的.

主要方法:

文章识别和验证.
通过出版商的系统发出纠正通知.

主要成果:

在DOI 10.1016/j.ymgmr.2023.101031已被纠正.
这样可以确保正确的链接和访问预期的研究.

结论:

校正维护科学出版物的可追溯性和完整性.
准确的DOI对于科学复制性和进步至关重要.

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

Functional Characterization of Endogenously Expressed Human RYR1 Variants

Functional Characterization of Endogenously Expressed Human RYR1 Variants

Published on: June 9, 2021

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