Proteomics Study of Peripheral Blood Mononuclear Cells in Down Syndrome Children

Down syndrome (DS) is the most common chromosomal disorder and the leading genetic cause of intellectual disability in humans, which results from the triplication of chromosome 21. To search for biomarkers for the early detection and exploration of the disease mechanisms, here, we investigated the p...

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Main Authors: Chiara Lanzillotta (Author), Viviana Greco (Author), Diletta Valentini (Author), Alberto Villani (Author), Valentina Folgiero (Author), Matteo Caforio (Author), Franco Locatelli (Author), Sara Pagnotta (Author), Eugenio Barone (Author), Andrea Urbani (Author), Fabio Di Domenico (Author), Marzia Perluigi (Author)
Format: Book
Published: MDPI AG, 2020-11-01T00:00:00Z.
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