Preuss, Natalie <br/><br/>
PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease.  [electronic resource] 

 -  Pediatric research  Jun 2002 
 - 706-14 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0031-3998 
<br/><br/><label>Standard No.: </label>10.1203/00006450-200206000-00008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATPases Associated with Diverse Cellular Activities<br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Fatty Acids--blood<br/>Genetic Complementation Test<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Membrane Proteins--genetics<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Severity of Illness Index<br/>Zellweger Syndrome--genetics