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CORRECTION article

Front. Neurol.
Sec. Neuromuscular Disorders and Peripheral Neuropathies
Volume 15 - 2024 | doi: 10.3389/fneur.2024.1512459

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

Provisionally accepted
Shijia Ouyang Shijia Ouyang 1Xiaoyin Peng Xiaoyin Peng 2Wenchen Huang Wenchen Huang 1Jinli Bai Jinli Bai 1Hong Wang Hong Wang 1Yuwei Jin Yuwei Jin 1Hui Jiao Hui Jiao 2Maoti Wei Maoti Wei 3Xiushan Ge Xiushan Ge 2Fang Song Fang Song 1Yujin Qu Yujin Qu 1*
  • 1 Capital Institute of Pediatrics, Beijing, Beijing Municipality, China
  • 2 Children's Hospital of Capital Institute of Pediatrics, Beijing, Beijing Municipality, China
  • 3 TEDA International Cardiovascular Hospital, Tianjin, China

The final, formatted version of the article will be published soon.

    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] 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: 10.1097/01.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.

    Keywords: spinal muscular atrophy, biomarkers, severity, motor milestones, Survival

    Received: 16 Oct 2024; Accepted: 17 Oct 2024.

    Copyright: © 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) or licensor 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: Yujin Qu, Capital Institute of Pediatrics, Beijing, Beijing Municipality, China

    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.