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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...
Uloženo v:
| Vydáno v: | Orphanet J Rare Dis |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6237029/ https://ncbi.nlm.nih.gov/pubmed/30428914 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-018-0938-8 |
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