- Open Access
Erratum to: “Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma”
© The Author(s). 2017
- 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 , 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.
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.
- 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:10.1186/s13148-015-0167-0.View ArticlePubMedPubMed CentralGoogle Scholar