UMD-MEN1 database: an overview of the 370 MEN1 variants present in 1,676 patients from the French population.
Fiche publication
Date publication
octobre 2018
Journal
The Journal of clinical endocrinology and metabolism
Auteurs
Membres identifiés du Cancéropôle Est :
Dr GOUDET Pierre
Tous les auteurs :
Romanet P, Mohamed A, Giraud S, Odou MF, North MO, Pertuit M, Pasmant E, Coppin L, Guien C, Calender A, Borson-Chazot F, Béroud C, Goudet P, Barlier A
Lien Pubmed
Résumé
Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant disease caused by mutations in the MEN1 gene characterized by a broad spectrum of clinical manifestations, of which the most frequent are primary hyperparathyroidism, pituitary adenomas, and neuroendocrine tumors.
Référence
J. Clin. Endocrinol. Metab.. 2018 Oct 18;: