Associated Papers
Identification of novel compound heterozygous variants in the PEX10 gene in a Han-Chinese family with PEX10-related peroxisome biogenesis disorders.
Huang X et al.
Plos One, 2025
How to Detect Isolated PEX10-Related Cerebellar Ataxia?
Nava E et al.
Neuropediatrics, 2022
PEX10-related autosomal recessive cerebellar ataxia with hearing loss.
Kaya Özçora GD et al.
Acta Neurologica Belgica, 2020
A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.
George AJ et al.
Frontiers in Genetics, 2018
29491882 (PubMed )
Supplement: Table2.xlsx › Sheet1
Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report.
Blomqvist M et al.
Journal of Medical Case Reports, 2017
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