Steinberg, S J <br/><br/>
Complementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder.  [electronic resource] 

 -  Journal of medical genetics  Apr 1996 
 - 295-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.33.4.295  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Catalase--analysis<br/>Cells, Cultured<br/>Fatty Acids--blood<br/>Fibroblasts--enzymology<br/>Genetic Complementation Test<br/>Humans<br/>Peroxisomal Disorders--genetics<br/>Phenotype<br/>Plasmalogens--biosynthesis<br/>Solubility