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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| 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 |