Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes

In familial cutaneous malignant melanoma (CMM), disruption of the retinoblastoma (pRB) pathway frequently occurs through inactivating mutations in the p16 (p16(INK4A)/CDKN2A/MTS1) gene or activating mutations in the G1-specific cyclin dependent kinase 4 gene (CDK4). Uveal malignant melanoma (UMM) al...

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Detalles Bibliográficos
Autores principales: Soufir, N, Bressac-de Paillerets, B, Desjardins, L, Lévy, C, Bombled, J, Gorin, I, Schlienger, P, Stoppa-Lyonnet, D
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374387/
https://www.ncbi.nlm.nih.gov/pubmed/10732752
http://dx.doi.org/10.1054/bjoc.1999.1005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374387/
https://www.ncbi.nlm.nih.gov/pubmed/10732752
http://dx.doi.org/10.1054/bjoc.1999.1005

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