RF27 | LBSUN362 Germline CDKN1B Variants Type And Site Are Associated With Specific Phenotype In Multiple Endocrine Neoplasia 4

BACKGROUND: The latest of the multiple endocrine neoplasia (MEN) syndromes described is MEN4, caused by germline CDKN1B tumor suppressor gene mutation. The main clinical manifestations of MEN4 are primary hyperparathyroidism (PHPT), neuroendocrine tumors (NET) and pituitary adenomas (PitAd). CDKN1B...

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Detalles Bibliográficos
Autores principales: Halperin, Reut, Tirosh, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Tumor Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627980/
http://dx.doi.org/10.1210/jendso/bvac150.1865

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627980/
http://dx.doi.org/10.1210/jendso/bvac150.1865

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