A homozygous PRDX3 pathogenic variant in a paediatric case of spinocerebellar ataxia type 32
Neurogenetics. 2025 Dec 6;26(1):86. doi: 10.1007/s10048-025-00869-w. ABSTRACT Spinocerebellar ataxia type 32 (SCAR32) is a rare autosomal neurodegenerative disorder caused by mutations in the peroxiredoxin 3 …