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Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX10 gene.
Biomarker and diagnostic research for peroxisome biogenesis disorder due to PEX10 defect has been reported in the published literature.
No clinical trials have been registered for peroxisome biogenesis disorder due to PEX10 defect.
6 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX10 defect. Research spans Diagnostic / Biomarker (33%), Case Report / Case Series (33%), and Review / Meta-Analysis (17%).
Correia J (2026). [PMID: 40632619](https://pubmed.ncbi.nlm.nih.gov/40632619/). *The journals of gerontology. Series A, Biological sciences and medical sciences*. [Basic Science / Preclinical]
Vercaemst A (2026). [PMID: 41677620](https://pubmed.ncbi.nlm.nih.gov/41677620/). *Cells*. [Diagnostic / Biomarker]
Huang X (2025). [PMID: 40267090](https://pubmed.ncbi.nlm.nih.gov/40267090/). *PloS one*. [Case Report / Case Series]
Liu H (2025). [PMID: 40243840](https://pubmed.ncbi.nlm.nih.gov/40243840/). *The Journal of cell biology*. [Review / Meta-Analysis]
Alayoubi AM (2025). [PMID: 39757991](https://pubmed.ncbi.nlm.nih.gov/39757991/). *Annals of medicine*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 11:57 PM UTC
Xue H (2024). [PMID: 39009665](https://pubmed.ncbi.nlm.nih.gov/39009665/). *Scientific reports*. [Diagnostic / Biomarker]