https://www.selleckchem.com/pr....oducts/sar439859.htm
is, surveillance for endocrine dysfunction is required for early intervention and management. Pheochromocytomas are rare catecholamine-producing neuroendocrine tumours arising from chromaffin cells of the adrenal medulla or extra-adrenal sympathetic paraganglia. Recent studies have indicated that up to 40% of pheochromocytomas could be attributable to an inherited germline variant in an increasing list of susceptibility genes. Germline variants of the MYC-associated factor ( ) gene have been associated with familial pheochromocytomas
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