Pheochromocytomas and Paragangliomas, Genetically Diverse and Minimalist, All at Once!

Producción científica: Short surveyrevisión exhaustiva

32 Citas (Scopus)

Resumen

Pheochromocytomas and paragangliomas are infrequent, genetically heterogeneous neuroendocrine tumors. In this issue of Cancer Cell, Fishbein et al. report novel driver genes, pathogenic mechanisms, and markers of malignancy. Notably, the new findings support the long-held view that these tumors distinctively arise from a single driver event, either inherited or acquired.

Idioma originalEnglish (US)
Páginas (desde-hasta)159-161
Número de páginas3
PublicaciónCancer Cell
Volumen31
N.º2
DOI
EstadoPublished - feb 13 2017

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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