TY  - GEN
AU  - Matsumoto,Naomi
AU  - Tamura,Shigehiko
AU  - Furuki,Satomi
AU  - Miyata,Non
AU  - Moser,Ann
AU  - Shimozawa,Nobuyuki
AU  - Moser,Hugo W
AU  - Suzuki,Yasuyuki
AU  - Kondo,Naomi
AU  - Fujiki,Yukio
TI  - Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
SN  - 0002-9297
PY  - 2003///0924
KW  - Amino Acid Sequence
KW  - Animals
KW  - CHO Cells
KW  - Catalase
KW  - metabolism
KW  - Cell Line
KW  - Cricetinae
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Female
KW  - Gene Expression
KW  - Genetic Complementation Test
KW  - Genotype
KW  - Humans
KW  - Membrane Proteins
KW  - deficiency
KW  - Mice
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Peroxisomal Disorders
KW  - classification
KW  - Peroxisome-Targeting Signal 1 Receptor
KW  - Phenotype
KW  - Pregnancy
KW  - RNA, Messenger
KW  - Receptors, Cytoplasmic and Nuclear
KW  - Sequence Homology, Amino Acid
KW  - Temperature
KW  - Tissue Distribution
KW  - Transfection
KW  - Zellweger Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/377004
ER  -