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Vascular Occlusion Training for Inclusion Body Myositis: A Novel Therapeutic Approach
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Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using
Yan Lu1, Yu-Wei Da1, Yong-Biao Zhang2
1Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Frontiers in Neuroscience
|September 4, 2018
Summary
This study corrects a previous article DOI. The corrected DOI is 10.3389/fnins.2018.00329. Further details are available via the corrected citation.
Area of Science:
- Neuroscience
- Scientific Publishing
Background:
- A previous article published in this journal contained an incorrect Digital Object Identifier (DOI).
Purpose of the Study:
- To provide the correct DOI for the article.
Main Methods:
- Correction of the article's metadata.
Main Results:
- The Digital Object Identifier (DOI) for the article has been updated.
Conclusions:
- Researchers can now accurately access the intended article using the corrected DOI.
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