Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs). MEN1 is usually consequent to different germline and somatic mutations of the MEN1 tumor suppress...

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Detalhes bibliográficos
Publicado no:Front Endocrinol (Lausanne)
Main Authors: Mele, Chiara, Mencarelli, Monica, Caputo, Marina, Mai, Stefania, Pagano, Loredana, Aimaretti, Gianluca, Scacchi, Massimo, Falchetti, Alberto, Marzullo, Paolo
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Endocrinology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7708377/
https://ncbi.nlm.nih.gov/pubmed/33312161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.591501
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