Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life
✍ Scribed by Gonçalves, Tatiana D.; Toledo, Rodrigo A.; Sekiya, Tomoko; Matuguma, Sergio E.; Maluf Filho, Fauze; Rocha, Manoel S.; Siqueira, Sheila A. C.; Glezer, Andrea; Bronstein, Marcelo D.; Pereira, Maria A. A.; Jureidini, Ricardo; Bacchella, Telesforo; Machado, Marcel C. C.; Toledo, Sergio P. A.; Lourenço, Delmar M.
- Book ID
- 121855852
- Publisher
- Endocrine Society
- Year
- 2014
- Tongue
- English
- Weight
- 266 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0021-972X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of tumors of the parathyroids, pancreas, and anterior pituitary. The MEN1 gene, which was identified in 1997, consists of 10 exons that encode a 610-amino acid protein referred to as menin. M