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      UBE3Aren substratuak identifikatzen Angelman sindromearen ingurukoak argitzeko. 

      Ramirez Sanchez, Juan Manuel; Lectez, Benoit; Osinalde Moraleja, Nerea; Elu, Nagore; Mayor Martinez, Ugo (Servicio Editorial de la Universidad del País Vasco/Euskal Herriko Unibertsitatearen Argitalpen Zerbitzua, 2019)
      Angelman syndrome (AS) is a rare neurodevelopmental disease that results from loss of function of the maternal UBE3A gene. UBE3A codes for an E3 ubiquitin ligase, that coordinately with E1 and E2 enzymes, attaches ubiquitin ...