Peroxisome biogenesis disorders: Identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13

Biochemical and Biophysical Research Communications

Volumn 243, Issue 2, 1998, Pages 368-371

  Shimozawa, Nobuyuki ^a   Suzuki, Yasuyuki ^a   Zhang, Zhongyi ^a   Imamura, Atsushi ^a   Tsukamoto, Toshiro ^b   Osumi, Takashi ^b   Tateishi, Keita ^c   Okumoto, Kanji ^c   Fujiki, Yukio ^c   Orii, Tadao ^d   Barth, Peter G ^e   Wanders, Ronald J A ^e   Kondo, Naomi ^a  

^a GIFU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY OF HYOGO   (Japan)

^c KYUSHU UNIVERSITY   (Japan)

^d CHUBU GAKUIN UNIVERSITY   (Japan)

^e UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

Chinese hamster ovary cell; Complementation group; Peroxisome; Peroxisome biogenesis disorders; PEX gene

Indexed keywords

ANIMAL CELL; ARTICLE; BIOGENESIS; CASE REPORT; CHO CELL; CHONDRODYSPLASIA PUNCTATA; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; MALE; MUTANT; NONHUMAN; PEROXISOME; PRESCHOOL CHILD; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; YEAST;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS;

EID: 0032512540     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1997.8067     Document Type: Article

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