Associated Papers
Identification of a new frameshift homozygous variant of PEX3 gene in a preterm infant with profound global developmental delay and bilateral ptosis: a case report and updated literature review.
Su J et al.
Bmc Pediatrics, 2026
Zellweger syndrome with unusual findings: non-immune hydrops fetalis, dermal erythropoiesis and hypoplastic toe nails.
Dursun A et al.
Journal of Inherited Metabolic Disease, 2009
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.
Shimozawa N et al.
Human Molecular Genetics, 2000
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