Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: de novo mutation of the KIF1A gene, a new hope in prognosis

Publication date: Available online 6 August 2020Source: Neurología (English Edition)Author(s): S. Urtiaga Valle, B. Fournier Gil, M.S. Ramiro León, B. Martínez Menéndez

Source: Neurologia - August 13, 2020 Category: Neurology Source Type: research