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SUN-046 Identification of Clinical Predictors for Detection of Mutations in Multiple Endocrine Neoplasia Type 1

Context: Guidelines has systematically suggested genetic testing for a wide spectrum of phenotypes in order to confirm or exclude surely the diagnosis of multiple endocrine neoplasia type 1 (MEN1). However, the probability of find a germline MEN1 mutation has showed extremely variable (5-95%) when d...

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Bibliografiske detaljer
Udgivet i:J Endocr Soc
Main Authors: Urtremari, Betsaida, Carvalho, Rafael, Quedas, Elisangela P S, Lourenco, Delmar
Format: Artigo
Sprog:Inglês
Udgivet: Endocrine Society 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6552916/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-046
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