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Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX16 gene.
No clinical trials have been registered for peroxisome biogenesis disorder due to PEX16 defect.
5 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX16 defect. Research spans Basic Science / Preclinical (100%).
Wangler MF (2025). [PMID: 40498764](https://pubmed.ncbi.nlm.nih.gov/40498764/). *PloS one*. [Basic Science / Preclinical]
Gomez VA (2025). [PMID: 40621817](https://pubmed.ncbi.nlm.nih.gov/40621817/). *Disease models & mechanisms*. [Basic Science / Preclinical]
Manor J (2024). [PMID: 39386423](https://pubmed.ncbi.nlm.nih.gov/39386423/). *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]
Wangler MF (2024). [PMID: 38746221](https://pubmed.ncbi.nlm.nih.gov/38746221/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 9:06 PM UTC