RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database

BACKGROUND: Retinoblastoma, a prototype of hereditary cancer, is the most common intraocular tumour in children and potential cause of blindness from therapeutic eye ablation, second tumours in germ line carrier's survivors, and even death when left untreated. The molecular scanning of RB1 in s...

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Detalles Bibliográficos
Autores principales: Valverde, José R, Alonso, Javier, Palacios, Itziar, Pestaña, Ángel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1298292/
https://www.ncbi.nlm.nih.gov/pubmed/16269091
http://dx.doi.org/10.1186/1471-2156-6-53

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1298292/
https://www.ncbi.nlm.nih.gov/pubmed/16269091
http://dx.doi.org/10.1186/1471-2156-6-53

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