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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...
Autores principales: | Urtremari, Betsaida, Carvalho, Rafael, Quedas, Elisangela P S, Lourenco, Delmar |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552916/ http://dx.doi.org/10.1210/js.2019-SUN-046 |
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