Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1–3
- 1Department of Medical Genetics, Capital Institute of Pediatrics, Beijing, China
- 2Department of Neurology, Children's Hospital Affiliated to Capital Institute Pediatrics, Beijing, China
- 3Center of Clinical Epidemiology, TEDA International Cardiovascular Hospital, Tianjin, China
A corrigendum on
Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1–3
by Ouyang, S., Peng, X., Huang, W., Bai, J., Wang, H., Jin, Y., Jiao, H., Wei, M., Ge, X., Song, F., and Qu, Y. (2024). Front. Neurol. 15:1382410. doi: 10.3389/fneur.2024.1382410
In the published article, the reference for (14) was incorrectly written as: Zerres K. Natural history in proximal spinal muscular atrophy. Arch Neurol. (1995) 52:518–23. doi: 10.1001/archneur.1995.00540290108025.
It should be: Zerres K, Rudnik-Schöneborn S. Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications. Arch Neurol. (1995) 52:518–23. doi: 10.1001/archneur.1995.00540290108025.
The reference for (28) was incorrectly written as: Anderson K, Talbot K. Spinal muscular atrophies reveal motor neuron vulnerability to defects in ribonucleoprotein handling. Curr Opin Neurol. (2003) 16:595–9. doi: 10.1097/00019052-200310000-00005.
It should be: Anderson K, Talbot K. Spinal muscular atrophies reveal motor neuron vulnerability to defects in ribonucleoprotein handling. Curr Opin Neurol. (2003) 16:595–9. doi: 10.1097/01.wco.0000093102.34793.13.
The reference for (45) was incorrectly written as: Mazoyer S, Vijzelaar R, Snetselaar R, Clausen M, Mason AG, Rinsma M, et al. The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent. PLoS One. (2019) 14:e0220211. doi: 10.1371/journal.pone.0220211.
It should be: Vijzelaar R, Snetselaar R, Clausen M, Mason AG, Rinsma M, Zegers M, et al. The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent. PLoS One. (2019) 14:e0220211. doi: 10.1371/journal.pone.0220211.
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.
Keywords: spinal muscular atrophy, biomarkers, severity, motor milestones, survival
Citation: Ouyang S, Peng X, Huang W, Bai J, Wang H, Jin Y, Jiao H, Wei M, Ge X, Song F and Qu Y (2024) Corrigendum: Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1–3. Front. Neurol. 15:1512459. doi: 10.3389/fneur.2024.1512459
Received: 16 October 2024; Accepted: 17 October 2024;
Published: 29 October 2024.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2024 Ouyang, Peng, Huang, Bai, Wang, Jin, Jiao, Wei, Ge, Song and Qu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Fang Song, songf_558@263.net; Yujin Qu, hurry_qu@sina.com
†These authors have contributed equally to this work and share first authorship