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

The Original Article was published on 08 January 2016

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.

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  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:10.1186/s13148-015-0167-0.

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Correspondence to Luis Benítez-Bribiesca.

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The online version of the original article can be found under doi:10.1186/s13148-015-0167-0.

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Quiñonez-Silva, G., Dávalos-Salas, M., Recillas-Targa, F. et al. Erratum to: “Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma”. Clin Epigenet 9, 27 (2017). https://doi.org/10.1186/s13148-017-0323-9

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