Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Abstract

Peroxisome-biogenesis disorders (PBDs), including Zellweger syndrome (ZS), are autosomal recessive diseases caused by a deficiency in peroxisome assembly as well as by a malfunction of peroxisomes, among which>10 genotypes have been identified. We have isolated a human PEX16 cDNA (HsPEX16) by performing an expressed-sequence-tag homology search on a human… (More)

Topics

Figures and Tables

Sorry, we couldn't extract any figures or tables for this paper.