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This erratum corrects:

Erratum: Mimicking Ketonuria in the Ketogenesis Defect 3-Hydroxy-3-Methylglutaryl- Coenzyme A Lyase Deficiency: An Artefact in the Analysis of Urinary Organic Acids

Sass JO, Fernando M and Behringer S. Mimicking Ketonuria in the Ketogenesis Defect 3-Hydroxy-3-Methylglutaryl- Coenzyme A Lyase Deficiency: An Artefact in the Analysis of Urinary Organic Acids. Journal of Inborn Errors of Metabolism & Screening. 2018; 6:1-4. DOI: 10.1177/2326409818797361

It was noted that the submission date of the above-mentioned article was 28 December 2017, which was wrongly published as 28 December 2018.

Publication Dates

  • Publication in this collection
    2018
Latin American Society Inborn Errors and Neonatal Screening (SLEIMPN); Instituto Genética para Todos (IGPT) Rua Ramiro Barcelos, 2350, CEP: 90035-903, Porto Alegre, RS - Brasil, Tel.: 55-51-3359-6338, Fax: 55-51-3359-8010 - Porto Alegre - RS - Brazil
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