CORRECTION article

Front. Neurol., 29 October 2024

Sec. Neuromuscular Disorders and Peripheral Neuropathies

Volume 15 - 2024 | https://doi.org/10.3389/fneur.2024.1512459

Corrigendum: Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1–3

  • 1. Department of Medical Genetics, Capital Institute of Pediatrics, Beijing, China

  • 2. Department of Neurology, Children's Hospital Affiliated to Capital Institute Pediatrics, Beijing, China

  • 3. Center of Clinical Epidemiology, TEDA International Cardiovascular Hospital, Tianjin, China

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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.

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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

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

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Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

15 - 2024

Updates

Copyright

*Correspondence: Fang Song Yujin Qu

†These authors have contributed equally to this work and share first authorship

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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