Whole Exome Sequencing Identifies Novel Recurrently Mutated Genes in Patients with Splenic Marginal Zone Lymphoma

The pathogenesis of splenic marginal zone lymphoma (SMZL) remains largely unknown. Recent high-throughput sequencing studies have identified recurrent mutations in key pathways, most notably NOTCH2 mutations in >25% of patients. These studies are based on small, heterogeneous discovery cohorts, a...

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Detalles Bibliográficos
Autores principales: Parry, Marina, Rose-Zerilli, Matthew J. J., Gibson, Jane, Ennis, Sarah, Walewska, Renata, Forster, Jade, Parker, Helen, Davis, Zadie, Gardiner, Anne, Collins, Andrew, Oscier, David G., Strefford, Jonathan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862727/
https://www.ncbi.nlm.nih.gov/pubmed/24349473
http://dx.doi.org/10.1371/journal.pone.0083244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862727/
https://www.ncbi.nlm.nih.gov/pubmed/24349473
http://dx.doi.org/10.1371/journal.pone.0083244

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