Multiple endocrine neoplasia type 1

Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very high penetrance and an equal sex distribution. It occurs in approximately one in...

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Autors principals: Marini, Francesca, Falchetti, Alberto, Monte, Francesca Del, Sala, Silvia Carbonell, Gozzini, Alessia, Luzi, Ettore, Brandi, Maria Luisa
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2006
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1594566/
https://ncbi.nlm.nih.gov/pubmed/17014705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-38
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