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Peroxins

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Clinically relevant AAV8- <i>PEX1</i> gene therapy preserves retinal integrity and function long-term in a murine model of Zellweger spectrum disorder
Peroxins
PEX11 mediates intralumenal vesicle formation in peroxisomes.
Peroxins
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.
Peroxins
Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi families.
Peroxins
Mitochondria and Peroxisome Crosstalk in Peroxisome Biogenesis Disorder 8A Caused by a Rare Variant in PEX16 Gene.
Peroxins
A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate.
Peroxins
Geographic characterization of RPE structure and lipid changes in the PEX1-p.Gly844Asp mouse model for Zellweger spectrum disorder
Peroxins
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 update literature review
Peroxins
Systematic study of ophthalmological findings in 10 patients with PEX1-mediated Zellweger spectrum disorder.
Peroxins
Hansenula polymorpha cells lacking the ER-localized peroxins Pex23 or Pex29 show defects in mitochondrial function and morphology.
Peroxins

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