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

Orphanet Journal of Rare Diseases volume 17, Article number: 21 (2022) Cite this article

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)
Full size table

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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Authors and Affiliations

  1. Center of Neonatal Disease Screening, Quanzhou Maternity and Children’s Hospital, 700 Fengze Street, Quanzhou, 362000, Fujian Province, China

    Yiming Lin, Yanru Chen, Zhenzhu Zheng, Qingliu Fu & Weihua Lin

  2. Administrative Office, Quanzhou Maternity and Children’s Hospital, 700 Fengze Street, Quanzhou, 362000, Fujian Province, China

    Bangbang Lin

  3. Department of Neonatology, Quanzhou Maternity and Children’s Hospital, 700 Fengze Street, Quanzhou, 362000, Fujian Province, China

    Weifeng Zhang

Authors
  1. Yiming Lin
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  2. Bangbang Lin
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  3. Yanru Chen
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  4. Zhenzhu Zheng
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  5. Qingliu Fu
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  6. Weihua Lin
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  7. Weifeng Zhang
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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

Orphanet Journal of Rare Diseases

ISSN: 1750-1172