Involvement of Foxp2 in the alterations of the basal ganglia circuitry in Huntington’s Disease 

Rodríguez Urgellés, Ened (Date of defense: 2022-01-20)

Huntington’s Disease (HD) is an autosomal dominant inherited neurodegenerative disorder characterized by motor, psychiatric, and cognitive manifestations. The disease is caused by an unstable expansion of the CAG trinucleotide ...