Correction to: implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns

Sonia Pajares^{1

2}, Jose Antonio Arranz³, Aida Ormazabal^{2

4}, Mireia Del Toro³, Ángeles García-Cazorla^{2

4}, Aleix Navarro-Sastre¹, Rosa María López^{1

5}, Silvia María Meavilla⁴, Mariela Mercedes de Los Santos⁴, Camila García-Volpe⁴, Jose Manuel González de Aledo-Castillo¹, Ana Argudo¹, Jose Luís Marín¹, Clara Carnicer³, Rafael Artuch^{2

4}, Frederic Tort^{1

2

5}, Laura Gort^{1

2

5}, Rosa Fernández⁶, Judit García-Villoria^#^{1

2

5}, Antonia Ribes^#^{7

8

9}

Affiliations

¹ Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
² Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain.
³ Unit of Metabolic Diseases, Hospital Vall D'Hebrón, Barcelona, Spain.
⁴ Inborn Errors of Metabolism Unit, Hospital Sant Joan de Déu, Barcelona, Spain.
⁵ Biomedical Research Institute, August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
⁶ Maternal and Child Health Service, Public Health Agency of Catalonia, Health Department, Government of Catalonia, Barcelona, Spain.
⁷ Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain. aribes@clinic.cat.
⁸ Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain. aribes@clinic.cat.
⁹ Biomedical Research Institute, August Pi I Sunyer (IDIBAPS), Barcelona, Spain. aribes@clinic.cat.

^# Contributed equally.

Published Erratum

Sonia Pajares et al. Orphanet J Rare Dis. 2023.

. 2023 Jul 13;18(1):188.

doi: 10.1186/s13023-023-02793-4.

¹ Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
² Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain.
³ Unit of Metabolic Diseases, Hospital Vall D'Hebrón, Barcelona, Spain.
⁴ Inborn Errors of Metabolism Unit, Hospital Sant Joan de Déu, Barcelona, Spain.
⁵ Biomedical Research Institute, August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
⁶ Maternal and Child Health Service, Public Health Agency of Catalonia, Health Department, Government of Catalonia, Barcelona, Spain.
⁷ Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain. aribes@clinic.cat.
⁸ Center for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain. aribes@clinic.cat.
⁹ Biomedical Research Institute, August Pi I Sunyer (IDIBAPS), Barcelona, Spain. aribes@clinic.cat.

^# Contributed equally.

No abstract available

Erratum for

Implementation of second-tier tests in newborn screening for the detection of vitamin B₁₂ related acquired and genetic disorders: results on 258,637 newborns.
Pajares S, Arranz JA, Ormazabal A, Del Toro M, García-Cazorla Á, Navarro-Sastre A, López RM, Meavilla SM, de Los Santos MM, García-Volpe C, de Aledo-Castillo JMG, Argudo A, Marín JL, Carnicer C, Artuch R, Tort F, Gort L, Fernández R, García-Villoria J, Ribes A. Pajares S, et al. Orphanet J Rare Dis. 2021 Apr 30;16(1):195. doi: 10.1186/s13023-021-01784-7. Orphanet J Rare Dis. 2021. PMID: 33931066 Free PMC article.

1. Pajares et al. (2021) Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns (2021). 16:195 DOI: 10.1186/s13023-021-01784-7. - PMC - PubMed