Orphanet Journal of Rare Diseases (Jan 2022)

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

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

DOI
https://doi.org/10.1186/s13023-022-02173-4
Journal volume & issue
Vol. 17, no. 1
pp. 1 – 3

Abstract

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