CORRECTION article

Front. Neurol., 08 September 2021

Sec. Neurogenetics

Volume 12 - 2021 | https://doi.org/10.3389/fneur.2021.756038

Corrigendum: HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade

  • 1. Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan

  • 2. Department of Medical Technology, Graduate School of Health Sciences, Niigata University, Niigata, Japan

  • 3. Division of Legal Medicine, Niigata University, Niigata, Japan

  • 4. Department of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan

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In the original article, there were mistakes in Figures 1 and 3 as published. The multiplier of the unit for protease activity was incorrect. The correct value is 10 to the third power. The corrected Figures 1 and 3 appear below.

Figure 1

Figure 3

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Summary

Keywords

heritability, vascular dementia, mutations, HTRA1, carriers, CARASIL

Citation

Uemura M, Nozaki H, Koyama A, Sakai N, Ando S, Kanazawa M, Kato T and Onodera O (2021) Corrigendum: HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade. Front. Neurol. 12:756038. doi: 10.3389/fneur.2021.756038

Received

09 August 2021

Accepted

10 August 2021

Published

08 September 2021

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

12 - 2021

Updates

Copyright

*Correspondence: Osamu Onodera

This article was submitted to Neurogenetics, a section of the journal Frontiers in Neurology

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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