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Items: 3

1.
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
D S Warren, J C Morrell, H W Moser, D Valle, S J Gould
Am J Hum Genet. 1998 Aug; 63(2): 347–359. doi: 10.1086/301963
PMCID:
PMC1377304
SummaryPDF–1.5M
2.
Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G
Ania C. Muntau, Peter U. Mayerhofer, Barbara C. Paton, Stefan Kammerer, Adelbert A. Roscher
Am J Hum Genet. 2000 Oct; 67(4): 967–975. Published online 2000 Aug 24. doi: 10.1086/303071
PMCID:
PMC1287898
AbstractArticlePDF–1.0M
3.
PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p
Kanji Okumoto, Nobuyuki Shimozawa, Atsusi Kawai, Shigehiko Tamura, Toshiro Tsukamoto, Takashi Osumi, Hugo Moser, Ronald J. A. Wanders, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki
Mol Cell Biol. 1998 Jul; 18(7): 4324–4336. doi: 10.1128/mcb.18.7.4324
PMCID:
PMC109016
AbstractArticlePDF–3.3M

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