https://www.selleckchem.com/products/PLX-4032.html
mber 2018.BACKGROUND Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder arising from mutations of the MEN1 tumor suppressor gene on chromosome 11q13; MEN1 is characterized by the development of neuroendocrine tumors, including those of the parathyroid, gastrointestinal endocrine tissue and anterior pituitary. Additionally, thymic neuroendocrine tumors in MEN1 are also rarely reported. CASE PRESENTATION This case report observed a family that presented with MEN1 p.L105Vfs mutation, and two of the family mem
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