Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients

BACKGROUND: Multiple endocrine neoplasia (MEN1) is a rare inherited multi-tumour syndrome, affecting specific neuroendocrine organs and non-endocrine tissues with a variable spectrum of over 20 possible different combinations, caused by inactivating heterozygote mutations of the MEN1 gene. Disease o...

Descripción completa

Detalles Bibliográficos
Autores principales: Marini, Francesca, Giusti, Francesca, Brandi, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237029/
https://www.ncbi.nlm.nih.gov/pubmed/30428914
http://dx.doi.org/10.1186/s13023-018-0938-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237029/
https://www.ncbi.nlm.nih.gov/pubmed/30428914
http://dx.doi.org/10.1186/s13023-018-0938-8

Ejemplares similares