Analysis of differentially expressed microRNAs in MEN1 parathyroid adenomas

Multiple Endocrine Neoplasia type 1 (MEN1) syndrome is a rare complex tumor-predisposing hereditary disorder, inherited in an autosomal dominant manner (OMIM 131100). MEN1 is characterized by tumors of the parathyroids, the neuroendocrine cells of the gastro-entero-pancreatic tract, and the anterior...

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Detaylı Bibliyografya
Yayımlandı:Am J Transl Res
Asıl Yazarlar: Luzi, Ettore, Ciuffi, Simone, Marini, Francesca, Mavilia, Carmelo, Galli, Gianna, Brandi, Maria Luisa
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: e-Century Publishing Corporation 2017
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5411922/
https://ncbi.nlm.nih.gov/pubmed/28469779
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