[PDF][PDF] Pheochromocytomas and paragangliomas, genetically diverse and minimalist, all at once!
PLM Dahia - Cancer Cell, 2017 - cell.com
PLM Dahia
Cancer Cell, 2017•cell.comPheochromocytomas 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.
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.
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.
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