# Neonatal adrenoleukodystrophy

> medical condition

**Wikidata**: [Q16965307](https://www.wikidata.org/wiki/Q16965307)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Neonatal_adrenoleukodystrophy)  
**Source**: https://4ort.xyz/entity/neonatal-adrenoleukodystrophy


## References

1. Monarch Disease Ontology release 2018-06-29
2. A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene
3. Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene
4. The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
5. The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes
6. PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders
7. Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders
8. Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
9. Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders