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 MEN1 gene predict clinical pre...

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Detalles Bibliográficos
Autores principales: Isailovic, Tatjana, Milicevic, Ivana, Macut, Djuro, Petakov, Milan, Ognjanovic, Sanja, Popovic, Bojana, Antic, Ivana Bozic, Bogavac, Tamara, Kovacevic, Valentina Elezovic, Ilic, Dusan, Damjanovic, Svetozar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298455/
https://www.ncbi.nlm.nih.gov/pubmed/30820182
http://dx.doi.org/10.2478/jomb-2018-0013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298455/
https://www.ncbi.nlm.nih.gov/pubmed/30820182
http://dx.doi.org/10.2478/jomb-2018-0013

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