Associated Papers
A homozygous PRDX3 pathogenic variant in a paediatric case of spinocerebellar ataxia type 32.
Yang J et al.
Neurogenetics, 2025
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40791678 (PubMed )
Supplement: media-2.xlsx › Table_S12_ClinVar_PLP_variants
Unraveling the genetic landscape of undiagnosed cerebellar ataxia in Brazilian patients.
Novis LE et al.
Parkinsonism & Related Disorders, 2024
Pure cerebellar ataxia due to bi-allelic PRDX3 variants including recurring p.Asp202Asn.
Efthymiou S et al.
Annals of Clinical and Translational Neurology, 2023
Exon Skipping Caused by Noncanonical Splicing Mutation in PRDX3-Related Spinocerebellar Ataxia.
Wang G et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2023
37553955 (PubMed )
Supplement: supplement_1.docx
A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.
Rafeeq MM et al.
Neurogenetics, 2023
Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3.
Martínez-Rubio D et al.
Human Molecular Genetics, 2022
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.
Rebelo AP et al.
Brain : a Journal of Neurology, 2021
Mutant Proteomics of Lung Adenocarcinomas Harboring Different EGFR Mutations.
Nishimura T et al.
Frontiers in Oncology, 2020
32983988 (PubMed )
Supplement: Data_Sheet_2.xlsx › AZ020
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