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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2005
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| 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 |