Correction to: Orphanet Journal of Rare Diseases (2021) 16:503 https://doi.org/10.1186/s13023-021-02126-3
Following the publication of the original article [1] the authors reported an error in Table 1 (page 3 of the PDF).
References 19 and 24 in the Table should be renumbered as 21 and 26 respectively.
The correct Table 1 is included in this Correction. The original article has been revised accordingly.
Reference
Lin, et al. Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening. Orphanet J Rare Dis. 2021;16:503. https://doi.org/10.1186/s13023-021-02126-3.
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Lin, Y., Lin, B., Chen, Y. et al. Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening. Orphanet J Rare Dis 17, 21 (2022). https://doi.org/10.1186/s13023-022-02173-4
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DOI: https://doi.org/10.1186/s13023-022-02173-4