Brief ReportsAssignment of the Human Peroxisome Assembly Factor-1 Gene (PXMP3) Responsible for Zellweger Syndrome to Chromosome 8q21.1 by Fluorescence in Situ Hybridization
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Cited by (13)
Genomic organization and characterization of human PEX2 encoding a 35-kDa peroxisomal membrane protein
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2011, Atlas of Inherited Metabolic Diseases: Third EditionSummary of heritable ocular disorders and selected systemic conditions with eye findings
2000, Ophthalmic GeneticsTransmembrane topology of the peroxin, Pex2p, an essential component for the peroxisome assembly
1999, Journal of Biochemistry
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