Whole exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas

Pheochromocytomas and paragangliomas (PCC/PGL) are the solid tumor type most commonly associated with an inherited susceptibility syndrome. However, very little is known about the somatic genetic changes leading to tumorigenesis or malignant transformation. Here we perform whole exome sequencing on...

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Dades bibliogràfiques
Publicat a:Nat Commun
Autors principals: Fishbein, Lauren, Khare, Sanika, Wubbenhorst, Bradley, DeSloover, Daniel, D’Andrea, Kurt, Merrill, Shana, Cho, Nam Woo, Greenberg, Roger A., Else, Tobias, Montone, Kathleen, LiVolsi, Virginia, Fraker, Douglas, Daber, Robert, Cohen, Debbie L., Nathanson, Katherine L.
Format: Artigo
Idioma:Inglês
Publicat: 2015
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4302757/
https://ncbi.nlm.nih.gov/pubmed/25608029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms7140
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