Open Access

Erratum to: “Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma”

  • Guadalupe Quiñonez-Silva1,
  • Mercedes Dávalos-Salas2,
  • Félix Recillas-Targa2,
  • Patricia Ostrosky-Wegman3,
  • Diego Arenas Aranda1 and
  • Luis Benítez-Bribiesca4Email author
Clinical EpigeneticsThe official journal of the Clinical Epigenetics Society20179:27

https://doi.org/10.1186/s13148-017-0323-9

Received: 2 February 2017

Accepted: 10 February 2017

Published: 16 March 2017

The original article was published in Clinical Epigenetics 2016 8:1

Following publication of this article [1], it has come to our attention that the following publication should have acknowledged Programa de Doctorado en Ciencias Biomédicas de la Universidad Nacional Autónoma de México for supporting the work.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Unidad de Investigación Médica en Genética Humana, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, IMSS
(2)
Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
(3)
Laboratorio de Genómica, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM)
(4)
Unidad de Investigación Médica en Enfermedades Oncológicas, Hospital de Oncología, CMNS-XXI, IMSS

Reference

  1. Quiñonez-Silva G, Dávalos-Salas M, Recillas-Targa F, Ostrosky-Wegman P, Aranda DA, Benítez-Bribiesca L. Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma. Clinical Epigenetics. 2016;8:1. doi:https://doi.org/10.1186/s13148-015-0167-0.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© The Author(s). 2017

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