Ferdinandusse, Sacha <br/><br/>
Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency.  [electronic resource] 

 -  Human mutation  Sep 2007 
 - 904-12 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.20535  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Oxidase<br/>Amino Acid Sequence<br/>Biomarkers--analysis<br/>Cells, Cultured<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Fatty Acids--analysis<br/>Fibroblasts--chemistry<br/>Genotype<br/>Humans<br/>Isoenzymes--genetics<br/>Lipid Metabolism, Inborn Errors--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>Oxidoreductases--genetics<br/>Peroxisomal Disorders--genetics<br/>Phenotype<br/>Sequence Homology, Amino Acid