Pheochromocytomas and paragangliomas (PCCs/PGLs) are rare neuroendocrine tumours with a significant genetic component. Here, the authors carry out a multi-omic integrative characterization of PCC/PGL and reveal potential genomic alterations and regulatory mechanisms involved in the disease.
- Luis Jaime Castro-Vega
- Eric Letouzé
- Anne-Paule Gimenez-Roqueplo