TY  - GEN
AU  - Ferdinandusse,Sacha
AU  - Denis,Simone
AU  - Hogenhout,Eveline M
AU  - Koster,Janet
AU  - van Roermund,Carlo W T
AU  - IJlst,Lodewijk
AU  - Moser,Ann B
AU  - Wanders,Ronald J A
AU  - Waterham,Hans R
TI  - Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency
SN  - 1098-1004
PY  - 2007///1002
KW  - Acyl-CoA Oxidase
KW  - Amino Acid Sequence
KW  - Biomarkers
KW  - analysis
KW  - Cells, Cultured
KW  - Cohort Studies
KW  - DNA Mutational Analysis
KW  - Fatty Acids
KW  - Fibroblasts
KW  - chemistry
KW  - Genotype
KW  - Humans
KW  - Isoenzymes
KW  - genetics
KW  - Lipid Metabolism, Inborn Errors
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Oxidoreductases
KW  - Peroxisomal Disorders
KW  - Phenotype
KW  - Sequence Homology, Amino Acid
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.20535
ER  -