Differential overexpression of SERPINA3 in human prion diseases
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DOI: 10.1038/s41598-017-15778-8
Abstract: Prion diseases are fatal neurodegenerative disorders with sporadic, genetic or acquired etiologies. The molecular alterations leading to the onset and the spreading of these diseases are still unknown. In a previous work we identified a… read more here.
Keywords: prion; overexpression serpina3; prion diseases; differential overexpression ... See more keywords