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Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX2 gene.
No clinical trials have been registered for peroxisome biogenesis disorder due to PEX2 defect.
12 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX2 defect. Research spans Basic Science / Preclinical (92%) and Case Report / Case Series (8%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 11 | 92% |
Patient case studies | 1 |
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 3:01 PM UTC
Manor J (2026). [PMID: 42098404](https://pubmed.ncbi.nlm.nih.gov/42098404/). *Commun Biol*. [Basic Science / Preclinical]
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]
Eberhart T (2026). [PMID: 41815956](https://pubmed.ncbi.nlm.nih.gov/41815956/). *Frontiers in molecular neuroscience*. [Basic Science / Preclinical]
Jiang CS (2025). [PMID: 39851575](https://pubmed.ncbi.nlm.nih.gov/39851575/). *Cells*. [Basic Science / Preclinical]
Khalilian S (2025). [PMID: 40205409](https://pubmed.ncbi.nlm.nih.gov/40205409/). *BMC medical genomics*. [Basic Science / Preclinical]
Gomez VA (2025). [PMID: 40621817](https://pubmed.ncbi.nlm.nih.gov/40621817/). *Disease models & mechanisms*. [Basic Science / Preclinical]
Wangler MF (2025). [PMID: 40498764](https://pubmed.ncbi.nlm.nih.gov/40498764/). *PloS one*. [Basic Science / Preclinical]
Wangler MF (2024). [PMID: 38746221](https://pubmed.ncbi.nlm.nih.gov/38746221/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
Gomez VA (2024). [PMID: 39605732](https://pubmed.ncbi.nlm.nih.gov/39605732/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
Pinelli M (2024). [PMID: 39069546](https://pubmed.ncbi.nlm.nih.gov/39069546/). *Cell death & disease*. [Basic Science / Preclinical]