Novel mutations in Serbian MEN1 patients: Genotype-phenotype correlation

Novel mutations in Serbian MEN1 patients: Genotype-phenotype correlation

Background: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome characterized by the occurrence of primary hyperparathyroidism (PHPT), pituitary adenoma (PA) and pancreatic neuroendocrine tumor (pNET). Whether the underlying mutations in M EN1 gene predict clinical pr...

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Bibliographic Details
Main Authors: Isailović Tatjana, Miličević Ivana, Macut Đuro, Petakov Milan, Ognjanović Sanja, Popović Bojana, Bozić-Antić Ivana, Bogavac Tamara, Elezović-Kovačević Valentina, Dušan Ilić, Damjanović Svetozar
Format: Article
Language:English
Published: Society of Medical Biochemists of Serbia, Belgrade 2019-01-01
Series:Journal of Medical Biochemistry
Subjects:
men 1
genotype
phenotype
novel mutations
Online Access:https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2019/1452-82581901038I.pdf

Internet

https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2019/1452-82581901038I.pdf

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