Literature DB >> 28331555

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, Luis Benítez-Bribiesca4.   

Abstract

[This corrects the article DOI: 10.1186/s13148-015-0167-0.].

Entities:  

Year:  2017        PMID： 28331555      PMCID： PMC5353778          DOI： 10.1186/s13148-017-0323-9

Source DB:  PubMed          Journal:  Clin Epigenetics        ISSN： 1868-7075            Impact factor:   6.551


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.  "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".

Authors:  Guadalupe Quiñonez-Silva; Mercedes Dávalos-Salas; Félix Recillas-Targa; Patricia Ostrosky-Wegman; Diego Arenas Aranda; Luis Benítez-Bribiesca
Journal:  Clin Epigenetics       Date:  2016-01-08       Impact factor: 6.551
  1 in total
  1 in total

Review 1.  DNA Methylation in the Diagnosis of Monogenic Diseases.

Authors:  Flavia Cerrato; Angela Sparago; Francesca Ariani; Fulvia Brugnoletti; Luciano Calzari; Fabio Coppedè; Alessandro De Luca; Cristina Gervasini; Emiliano Giardina; Fiorella Gurrieri; Cristiana Lo Nigro; Giuseppe Merla; Monica Miozzo; Silvia Russo; Eugenio Sangiorgi; Silvia M Sirchia; Gabriella Maria Squeo; Silvia Tabano; Elisabetta Tabolacci; Isabella Torrente; Maurizio Genuardi; Giovanni Neri; Andrea Riccio
Journal:  Genes (Basel)       Date:  2020-03-26       Impact factor: 4.096
  1 in total

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