Dual role of CDK5 on cognitive deficits and striatal vulnerability in Huntington’s disease 

Alvarez Periel, Elena (Date of defense: 2018-07-06)

Huntington’s disease (HD) is a neurodegenerative disorder caused by an autosomic mutation on the Huntingtin (HTT) coding gene. HD is mainly characterized by the appearance of motor symptoms or choreas, which are associated ...