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- W2108414634 abstract "About ten percent of pheochromocytomas are associated with familial syndrome. Hereditary pheochromocytoma has characteristics of early onset, multifocality and bilaterality. We experienced a case of 44-year-old man with bilateral pheochromocytoma without evidence of medullary thyroid cancer. Genetic test detected a L790F germline mutation of RET oncogene. The author found a necessity for genetic tests in cases of young-age, bilateral pheochromocytoma." @default.
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- W2108414634 date "2012-01-01" @default.
- W2108414634 modified "2023-09-27" @default.
- W2108414634 title "Bilateral adrenal pheochromocytoma with a germline L790F mutation in theREToncogene" @default.
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- W2108414634 doi "https://doi.org/10.4174/jkss.2012.82.3.185" @default.
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