TY  - GEN
AU  - Shimozawa,N
AU  - Suzuki,Y
AU  - Zhang,Z
AU  - Imamura,A
AU  - Tsukamoto,T
AU  - Osumi,T
AU  - Tateishi,K
AU  - Okumoto,K
AU  - Fujiki,Y
AU  - Orii,T
AU  - Barth,P G
AU  - Wanders,R J
AU  - Kondo,N
TI  - Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13
SN  - 0006-291X
PY  - 1998///0327
KW  - Animals
KW  - CHO Cells
KW  - Catalase
KW  - immunology
KW  - Chromosome Mapping
KW  - Cloning, Molecular
KW  - Cricetinae
KW  - DNA, Complementary
KW  - genetics
KW  - Fibroblasts
KW  - Fluorescent Antibody Technique
KW  - Genetic Complementation Test
KW  - Humans
KW  - Infant
KW  - Male
KW  - Membrane Proteins
KW  - Peroxisomal Disorders
KW  - Phenotype
KW  - Transfection
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1006/bbrc.1997.8067
ER  -