Newly identified milder phenotype of peroxisome biogenesis disorder caused by mutated PEX3 gene

A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly

Nobuyuki Shimozawa, Toshiro Tsukamoto, Yasuyuki Suzuki et al. · Science · 1992 · 360 citations

Peroxisome Assembly, Genetics, Molecular Biology +20

Insertion of the 70-kDa Peroxisomal Membrane Protein into Peroxisomal Membranes in Vivo and in Vitro

Tsuneo Imanaka, Yu'ichi Shiina, Tatsuya Takano et al. · Journal of Biological Chemistry · 1996 · 124 citations · Full text

Peroxisome Remnants in <i>pex3Δ</i> Cells and the Requirement of Pex3p for Interactions Between the Peroxisomal Docking and Translocation Subcomplexes

Partha Hazra, Ivet Suriapranata, William B. Snyder et al. · Traffic · 2002 · 116 citations · Full text

Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

Ania C. Muntau, Peter Mayerhofer, Barbara C. Paton et al. · The American Journal of Human Genetics · 2000 · 109 citations · Full text

Molecular Physiology, Mendelian Disorder, Complementation Group G +7

d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder

Yasuyuki Suzuki, Ling Jiang, Masayoshi Souri et al. · The American Journal of Human Genetics · 1997 · 107 citations · Full text

Aldehyde Dehydrogenase, Biochemistry, Peroxisomal Disorder +8