Abstract In the present study. we describe two novel cases of SCA5 with early onset. The first one. carrying a novel heterozygous de novo missense mutation in SPTBN2 gene. https://www.roneverhart.com/ASUS-R565EA-UH51T-15-6-FHD-1920x1080-Touch-Laptop-Intel-Core-i5-1135G7-2-4GHz-8GB-RAM-256GB-SSD-Windows-10/