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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Dades bibliogràfiques

Publicat a:	Mol Cell Biol
Autors principals:	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
Idioma:	Inglês
Publicat:	Taylor & Francis 1998
Matèries:	Cell and Organelle Structure and Assembly
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC109016/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9632816/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/mcb.18.7.4324
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