TREX1 and SAMHD1, and Aicardi-Goutières Syndrome 

    Valverde Estrella, Lorena (Date of defense: 2015-02-06)

    Aicardi-Goutières Syndrome (AGS) is a rare encephalopathy which mimics a viral intrauterine infection and is characterized by calcifications of the basal ganglia, cerebral atrophy and IFN-a in the cerebrospinal fluid. AGS ...