Incidental finding of MEN-1 syndrome during staging and follow-up of breast carcinoma

Type 1 multiple endocrine neoplasia (MEN-1) syndrome is an autosomal dominant disease, associated with germline mutations in the MEN-1 tumour suppressor gene (encoding the menin protein). Recent studies, through a better characterisation of the functions of the menin protein, have started to demonst...

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Detalles Bibliográficos
Autores principales: Maria, Bernardo Conde, Quadros, Ana Catarina, Alves, Natália, Coutinho, João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754650/
https://www.ncbi.nlm.nih.gov/pubmed/33370954
http://dx.doi.org/10.1136/bcr-2020-238784

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754650/
https://www.ncbi.nlm.nih.gov/pubmed/33370954
http://dx.doi.org/10.1136/bcr-2020-238784

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