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Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening

The Original Article was published on 04 December 2021

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).

Table 1 Biochemical and genetic characteristics of 49 patients with primary carnitine deficiency (PCD)

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

  1. 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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Correspondence to Weihua Lin or Weifeng Zhang.

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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