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

Rat PEX12 cDNA was isolated by functional complementation of peroxisome deficiency of a mutant CHO cell line, ZP109 (K. Okumoto, A. Bogaki, K. Tateishi, T. Tsukamoto, T. Osumi, N. Shimozawa, Y. Suzuki, T. Orii, and Y. Fujiki, Exp. Cell Res. 233:11–20, 1997), using a transient transfection assay and...

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Bibliographic Details
Main Authors: Okumoto, Kanji, Shimozawa, Nobuyuki, Kawai, Atsusi, Tamura, Shigehiko, Tsukamoto, Toshiro, Osumi, Takashi, Moser, Hugo, Wanders, Ronald J. A., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Format: Artigo
Language:Inglês
Published: American Society for Microbiology 1998
Subjects:
Cell and Organelle Structure and Assembly
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC109016/
https://ncbi.nlm.nih.gov/pubmed/9632816
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