Associated Papers
Identification of a novel heterozygous variant in the PEX26 gene in an infant: a case report.
Huang Y et al.
Translational Pediatrics, 2024
Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency.
Lotz-Havla AS et al.
Frontiers in Genetics, 2021
34804114 (PubMed )
Supplement: DataSheet1.pdf
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder.
Ebberink MS et al.
Human Mutation, 2011
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.
Weller S et al.
American Journal of Human Genetics, 2005
Select a paper to view details