Correction: Orphanet Journal of Rare Diseases (2023) 18:102 https://doi.org/10.1186/s13023-023-02673-x
Following publication of the original article [1], we have been notified that the affiliation 5 (Key Laboratory of Digital Technology in Medical Diagnostics of Zhejiang Province, Zhejiang, China) should not be assigned to author Guoli Tian. Also, statement of equal contribution is missing. It should be as follows:
Guoli Tian3*
Zhixing Zhu and Georgi Z. Genchev are first co-authors with equal contribution.
Reference
Zhu Z, et al. Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients. Orphanet J Rare Dis. 2023;18:102. https://doi.org/10.1186/s13023-023-02673-x.
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Zhu, Z., Genchev, G.Z., Wang, Y. et al. Correction: Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients. Orphanet J Rare Dis 18, 150 (2023). https://doi.org/10.1186/s13023-023-02752-z
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DOI: https://doi.org/10.1186/s13023-023-02752-z