Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring
- PMID: 38510379
- PMCID: PMC10953821
- DOI: 10.3389/fneur.2024.1376447
Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring
Abstract
[This corrects the article DOI: 10.3389/fneur.2022.1072256.].
Keywords: Aicardi-Goutières syndrome (AGS); C26:0-lysophosphatidylcholine; DBS; X-ALD; X-linked adrenoleukodystrophy (X-ALD); Zellweger Spectrum Disorders; hematopoietic stem cell transplantation (HCST); newborn screening (NBS).
Copyright © 2024 Bonaventura, Alberti, Lucchi, Cappelletti, Fazzone, Cattaneo, Bellini, Izzo, Parazzini, Bosetti, Di Profio, Fiore, Ferrario, Mameli, Sangiorgio, Masnada, Zuccotti, Veggiotti, Spaccini, Iascone, Verduci, Cereda, Tonduti and XALD-NBS Study Group.
Erratum for
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Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring.Front Neurol. 2023 Jan 9;13:1072256. doi: 10.3389/fneur.2022.1072256. eCollection 2022. Front Neurol. 2023. PMID: 36698902 Free PMC article.
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