Publication | Open Access

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

Biallelic MutationsNeurological DisorderStriatal Pde10aParkinson DiseaseCorticobasal DegenerationDegenerative DiseaseMotor DisorderPde10a LeadNeurologyNeuroscienceStereotypic Movement DisorderMedicineMovement Disorders