Novel genetic mutations within the VPS13D gene cause a novel case of autosomal recessive spinocerebellar ataxia type 4 (SCAR4)
Nerea Ramírez
Neurogenetics
Date and time: | 9:30-10:00
Venue: Sala Polivalent, IGTP Mar and online
This coffee talk will be held in person, but if you're unable to attend, you can join online.