Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: Identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

被引:51
|
作者
Shimozawa, N
Suzuki, Y
Zhang, Z
Imamura, A
Kondo, N
Kinoshita, N
Fujiki, Y
Tsukamoto, T
Osumi, T
Imanaka, T
Orii, T
Beemer, F
Mooijer, P
Dekker, C
Wanders, RJA
机构
[1] Gifu Univ, Sch Med, Dept Pediat, Gifu 5008076, Japan
[2] Kyushu Univ, Fac Sci, Dept Biol, Fukuoka 812, Japan
[3] Himeji Inst Technol, Dept Life Sci, Himeji, Hyogo 67122, Japan
[4] Teikyo Univ, Fac Pharmaceut Sci, Dept Microbiol & Mol Pathol, Kanagawa, Japan
[5] Chubu Gakuin Univ, Fac Human Welfare, Seki, Japan
[6] Wilhelmina Childrens Hosp, Dept Clin Genet, Clin Genet Ctr, Utrecht, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Dept Clin Biochem & Pediat, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1086/302142
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:1898 / 1903
页数:6
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