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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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Detalhes bibliográficos
Main Authors: Schilling, Bastian, Bielefeld, Nicola, Sucker, Antje, Hillen, Uwe, Zimmer, Lisa, Schadendorf, Dirk, Zeschnigk, Michael, Griewank, Klaus G
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3671181/
https://ncbi.nlm.nih.gov/pubmed/23694694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-1596-8-87
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