Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene
<p>Abstract</p> <p>Background</p> <p>Retinoblastoma is caused by compound heterozygosity or homozygosity of retinoblastoma gene (<it>RB1</it>) mutations. In germline retinoblastoma, mutations in the <it>RB1 </it>gene predispose individuals to increased cancer risks during development. These mutation...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMC
2011-05-01
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| Saila: | BMC Medical Genetics |
| Sarrera elektronikoa: | http://www.biomedcentral.com/1471-2350/12/76 |
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