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CORRECTION article

Front. Genet., 30 September 2021
Sec. Genetics of Common and Rare Diseases

Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele

  • 1Laboratorio de Glicobiología Humana y Diagnóstico Molecular, Centro de Investigación en Dinámica Celular, Instituto de Investigación en Ciencias Básicas y Aplicadas, Universidad Autónoma del Estado de Morelos, Cuernavaca, Mexico
  • 2Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Mexico
  • 3Programa de Maestría y Doctorado en Ciencias Médicas, Universidad Nacional Autónoma de México (UNAM), Ciudad Universitaria, Mexico City, Mexico
  • 4Laboratorio de Citogenética, Instituto Nacional de Pediatría, Mexico City, Mexico
  • 5Centro de Rehabilitación e Inclusión Infantil Teletón, Tuxtla Gutiérrez, Mexico
  • 6Hospital Regional de Alta Especialidad Ciudad Salud, Tapachula, Mexico
  • 7Palmieri Metabolic Disease Laboratory, Children’s Hospital of Philadelphia, Philadelphia, PA, United States
  • 8Department of Laboratory Medicine and Pathology, Laboratory Genetics and Genomics, Mayo Clinic, Rochester, MN, United States
  • 9Genos Médica, Mexico City, Mexico
  • 10Laboratorio de Diagnóstico Genómico, Instituto Nacional de Medicina Genómica, Secretaría de Salud, Mexico City, Mexico
  • 11Laboratorio de Inmunología Molecular, Facultad de Medicina, Universidad Autónoma del Estado de Morelos, Cuernavaca, Mexico
  • 12Departamento de Neurología, Instituto Nacional de Pediatría, Mexico City, Mexico
  • 13Human Genetics Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, United States
  • 14Departamento de Biología, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Mexico
  • 15Sociedad Latinoamericana de Glicobiología A.C, Cuernavaca, Mexico

A corrigendum on

ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele

by González-Domínguez, C. A., Fiesco-Roa, M. O., Gómez-Carmona, S., Kleinert-Altamirano, A. P. I., He, M., Daniel, E. J. P, Raymond, K. M, Abreu-González, M., Manrique-Hernández, S., González-Jaimes, A., Salinas-Marín, R., Molina-Garay, C., Carrillo-Sánchez, K., Flores-Lagunes, L. L., Jiménez-Olivares, M., Muñoz-Rivas, A., Cruz-Muñoz, M. E., Ruíz-García, M., Freeze, H. H., Mora-Montes, H. M., Alaez-Verson, C., and Martínez-Duncker, I. (2021). Front. Genet:12: 744884. doi: 10.3389/fgene.2021.744884

In the published article, there were errors regarding the affiliations for Anke Paula Ingrid Kleinert-Altamirano, Earnest James Paul Daniel, and Miao He.

Anke Paula Ingrid Kleinert-Altamirano should have affiliations 5 “Centro de Rehabilitación e Inclusión Infantil Teletón, Tuxtla Gutiérrez, Mexico” and 7 “Hospital Regional de Alta Especialidad Ciudad Salud, Tapachula, Mexico” instead of 5 and 6.

Miao He and Earnest James Paul Daniel should have affiliation 6 “Palmieri Metabolic Disease Laboratory, Children’s Hospital of Philadelphia, Philadelphia, PA, United States” instead of 7.

The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: CDG, splicing, metabolic, glycosylation, ALG1, mutation, tetrasaccharide

Citation: González-Domínguez CA, Fiesco-Roa MO, Gómez-Carmona S, Kleinert-Altamirano API, He M, Daniel EJP, Raymond KM, Abreu-González M, Manrique-Hernández S, González-Jaimes A, Salinas-Marín R, Molina-Garay C, Carrillo-Sánchez K, Flores-Lagunes LL, Jiménez-Olivares M, Muñoz-Rivas A, Cruz-Muñoz ME, Ruíz-García M, Freeze HH, Mora-Montes HM, Alaez-Verson C and Martínez-Duncker I (2021) Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele. Front. Genet. 12:777731. doi: 10.3389/fgene.2021.777731

Received: 15 September 2021; Accepted: 16 September 2021;
Published: 30 September 2021.

Approved by:

Frontiers in Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2021 González-Domínguez, Fiesco-Roa, Gómez-Carmona, Kleinert-Altamirano, He, Daniel, Raymond, Abreu-González, Manrique-Hernández, González-Jaimes, Salinas-Marín, Molina-Garay, Carrillo-Sánchez, Flores-Lagunes, Jiménez-Olivares, Muñoz-Rivas, Cruz-Muñoz, Ruíz-García, Freeze, Mora-Montes, Alaez-Verson and Martínez-Duncker. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Iván Martínez-Duncker, duncker@uaem.mx

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.