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<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title>Frontiers in Neurology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurol.</abbrev-journal-title>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
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<article-meta>
<article-id pub-id-type="doi">10.3389/fneur.2024.1512459</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neurology</subject>
<subj-group>
<subject>Correction</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Corrigendum: Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1&#x02013;3</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Ouyang</surname> <given-names>Shijia</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Peng</surname> <given-names>Xiaoyin</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Huang</surname> <given-names>Wenchen</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Bai</surname> <given-names>Jinli</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Wang</surname> <given-names>Hong</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Jin</surname> <given-names>Yuwei</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Jiao</surname> <given-names>Hui</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Wei</surname> <given-names>Maoti</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/2754108/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Ge</surname> <given-names>Xiushan</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1502042/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Song</surname> <given-names>Fang</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Qu</surname> <given-names>Yujin</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/2556650/overview"/>
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<aff id="aff1"><sup>1</sup><institution>Department of Medical Genetics, Capital Institute of Pediatrics</institution>, <addr-line>Beijing</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Neurology, Children&#x00027;s Hospital Affiliated to Capital Institute Pediatrics</institution>, <addr-line>Beijing</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>Center of Clinical Epidemiology, TEDA International Cardiovascular Hospital</institution>, <addr-line>Tianjin</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Fang Song <email>songf_558&#x00040;263.net</email></corresp>
<corresp id="c002">Yujin Qu <email>hurry_qu&#x00040;sina.com</email></corresp>
<fn fn-type="equal" id="fn002"><p>&#x02020;These authors have contributed equally to this work and share first authorship</p></fn></author-notes>
<pub-date pub-type="epub">
<day>29</day>
<month>10</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1512459</elocation-id>
<history>
<date date-type="received">
<day>16</day>
<month>10</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>10</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2024 Ouyang, Peng, Huang, Bai, Wang, Jin, Jiao, Wei, Ge, Song and Qu.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Ouyang, Peng, Huang, Bai, Wang, Jin, Jiao, Wei, Ge, Song and Qu</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>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.</p></license>
</permissions>
<related-article id="RA1" related-article-type="corrected-article" journal-id="Front. Neurol." journal-id-type="nlm-ta" vol="15" page="1382410" xlink:href="10.3389/fneur.2024.1382410" ext-link-type="doi">A corrigendum on <article-title>Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1&#x02013;3</article-title> 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). <italic>Front. Neurol</italic>. 15:1382410. doi: <object-id>10.3389/fneur.2024.1382410</object-id></related-article>
<kwd-group>
<kwd>spinal muscular atrophy</kwd>
<kwd>biomarkers</kwd>
<kwd>severity</kwd>
<kwd>motor milestones</kwd>
<kwd>survival</kwd>
</kwd-group>
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<page-count count="2"/>
<word-count count="627"/>
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<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Neuromuscular Disorders and Peripheral Neuropathies</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>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&#x02013;23. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1001/archneur.1995.00540290108025">10.1001/archneur.1995.00540290108025</ext-link>.</p>
<p>It should be: Zerres K, Rudnik-Sch&#x000F6;neborn S. Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications. <italic>Arch Neurol</italic>. (1995) 52:518&#x02013;23. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1001/archneur.1995.00540290108025">10.1001/archneur.1995.00540290108025</ext-link>.</p>
<p>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&#x02013;9. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1097/00019052-200310000-00005">10.1097/00019052-200310000-00005</ext-link>.</p>
<p>It should be: Anderson K, Talbot K. Spinal muscular atrophies reveal motor neuron vulnerability to defects in ribonucleoprotein handling. <italic>Curr Opin Neurol</italic>. (2003) 16:595&#x02013;9. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1097/01.wco.0000093102.34793.13">10.1097/01.wco.0000093102.34793.13</ext-link>.</p>
<p>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: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1371/journal.pone.0220211">10.1371/journal.pone.0220211</ext-link>.</p>
<p>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. <italic>PLoS One</italic>. (2019) 14:e0220211. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1371/journal.pone.0220211">10.1371/journal.pone.0220211</ext-link>.</p>
<p>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.</p>
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