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Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX19 gene.
No clinical trials have been registered for peroxisome biogenesis disorder due to PEX19 defect.
3 publications have been identified in PubMed for peroxisome biogenesis disorder due to PEX19 defect. Research spans Basic Science / Preclinical (67%) and Case Report / Case Series (33%).
de Lange EMF (2026). [PMID: 40847603](https://pubmed.ncbi.nlm.nih.gov/40847603/). *FEBS J*. [Basic Science / Preclinical]
Correia J (2026). [PMID: 40632619](https://pubmed.ncbi.nlm.nih.gov/40632619/). *J Gerontol A Biol Sci Med Sci*. [Basic Science / Preclinical]
Alayoubi AM (2025). [PMID: 39757991](https://pubmed.ncbi.nlm.nih.gov/39757991/). *Ann Med*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 8:55 PM UTC