Gärtner, J <br/><br/>
Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype.  [electronic resource] 

 -  Journal of inherited metabolic disease  May 1999 
 - 311-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1023/a:1005599903632  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATPases Associated with Diverse Cellular Activities<br/>Aspartic Acid--genetics<br/>Child<br/>Glycine--genetics<br/>Humans<br/>Infant<br/>Membrane Proteins--genetics<br/>Microbodies<br/>Mutation<br/>Peroxisomal Disorders--genetics<br/>Phenotype<br/>Zellweger Syndrome--genetics