Lack of SF3B1 R625 mutations in cutaneous melanoma

BACKGROUND: Melanoma is a deadly disease affecting people worldwide. Genetic studies have identified different melanoma subtypes characterized by specific recurrently mutated genes and led to the successful clinical introduction of targeted therapies. Hotspot mutations in SF3B1 were recently reporte...

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Detalles Bibliográficos
Autores principales: Schilling, Bastian, Bielefeld, Nicola, Sucker, Antje, Hillen, Uwe, Zimmer, Lisa, Schadendorf, Dirk, Zeschnigk, Michael, Griewank, Klaus G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671181/
https://www.ncbi.nlm.nih.gov/pubmed/23694694
http://dx.doi.org/10.1186/1746-1596-8-87

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671181/
https://www.ncbi.nlm.nih.gov/pubmed/23694694
http://dx.doi.org/10.1186/1746-1596-8-87

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