Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening (Orphanet Journal of Rare Diseases, (2021), 16, 1, (503), 10.1186/s13023-021-02126-3)

Yiming Lin; Bangbang Lin; Yanru Chen; Zhenzhu Zheng; Qingliu Fu; Weihua Lin; Weifeng Zhang

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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, (2021), 16, 1, (503), 10.1186/s13023-021-02126-3)

Orphanet Journal of Rare Diseases

DOI: 10.1186/s13023-022-02173-4

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Abstract

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.

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Lin, Y., Lin, B., Chen, Y., Zheng, Z., Fu, Q., Lin, W., & Zhang, W. (2022, December 1). Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening (Orphanet Journal of Rare Diseases, (2021), 16, 1, (503), 10.1186/s13023-021-02126-3). Orphanet Journal of Rare Diseases. BioMed Central Ltd. https://doi.org/10.1186/s13023-022-02173-4

Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening (Orphanet Journal of Rare Diseases, (2021), 16, 1, (503), 10.1186/s13023-021-02126-3)

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