RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling

Retinoblastoma (RB) is an inherited childhood ocular cancer caused by mutations in the tumor suppressor RB1 gene. Identification of RB1 mutations is essential to assess the risk of developing retinoblastoma in the patients´ relatives. Retinoblastoma is a potentially curable cancer and an early diagn...

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Detalles Bibliográficos
Autores principales: Parma, Diana, Ferrer, Marcela, Luce, Leonela, Giliberto, Florencia, Szijan, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738096/
https://www.ncbi.nlm.nih.gov/pubmed/29261756
http://dx.doi.org/10.1371/journal.pone.0189736

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738096/
https://www.ncbi.nlm.nih.gov/pubmed/29261756
http://dx.doi.org/10.1371/journal.pone.0189736

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