Differences in Menin Expression in Pituitary Adenomas in Multiple Endocrine Neoplasia Type 1, Its Phenocopies and Sporadic Acromegaly

Introduction: Multiple endocrine neoplasia type 1 syndrome (MEN 1) is caused by mutations in MEN1 gene, encoding menin protein. A combination of pituitary adenomas (PA) and primary hyperparathyroidism (PHPT) in patients without MEN1 mutations is defined as MEN 1 phenocopy. The aim of the study is to...

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Detalles Bibliográficos
Autores principales: Dimitrova, Diana A, Mamedova, Elizaveta O, Lapshina, Anastasia M, Azizyan, Vilen N, Grigoriev, Andrey Y, Vasilyev, Evgeny V, Tiulpakov, Anatoly N, Belaya, Zhanna E, Melnichenko, Galina A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Neuroendocrinology and Pituitary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090574/
http://dx.doi.org/10.1210/jendso/bvab048.1091

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090574/
http://dx.doi.org/10.1210/jendso/bvab048.1091

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