MON-923 MENIN Gene Mutation: Unity Amidst Diversity
نویسندگان
چکیده
منابع مشابه
Mutation of the MENIN gene in sporadic pancreatic endocrine tumors.
Pancreatic endocrine tumors occur both sporadically and as part of the multiple endocrine neoplasia type 1 (MEN1) syndrome. MEN1 is an autosomal dominant disease characterized by parathyroid hyperplasia, pancreatic endocrine tumors, and pituitary adenomas. The MEN1 gene called MENIN maps to chromosome 11q13 and is thought to function as a tumor suppressor gene. We previously demonstrated loss o...
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*Corresponding author: Pavan Malleshappa, Division of Nephrology, Department of Medicine, Adichunchanagiri Institute of Medical Sciences, B. G. nagara, Nagamangala Taluk, Mandya District, Karnataka State, India. E-mail: [email protected] C nephropathy refers to a disorder in which C1q deposits are seen in mesangium on immunofluorescence microscopy and mesangial electron dense deposits on el...
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ژورنال
عنوان ژورنال: Journal of the Endocrine Society
سال: 2020
ISSN: 2472-1972
DOI: 10.1210/jendso/bvaa046.1711