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Zellweger Syndrome; Identification of Mutations in PEX19 and PEX26 Gene in Saudi Families

Abdulfatah M. Alayoubi,Ambreen Ijaz,Abdul Wali,Jamil A. Hashmi, Azizah Alharbi,Sulman Basit

ANNALS OF MEDICINE（2025）

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Key words
Peroxisome biogenesis disorders,severe Zellweger spectrum disorder,whole exome sequencing,PEX19 gene,PEX26 gene
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