Van Veldhoven, P P <br/><br/>
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.  [electronic resource] 

 -  European journal of clinical investigation  Aug 2001 
 - 714-22 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0014-2972 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2362.2001.00877.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cells, Cultured<br/>Fatty Acids--chemical synthesis<br/>Female<br/>Fibroblasts--enzymology<br/>Humans<br/>Infant, Newborn<br/>Isomerism<br/>Malabsorption Syndromes--etiology<br/>Oxidation-Reduction<br/>Palmitic Acids--chemical synthesis<br/>Peroxisomal Disorders--enzymology<br/>Peroxisomes--enzymology<br/>Racemases and Epimerases--deficiency<br/>Skin--cytology<br/>Vitamin K Deficiency--etiology