Geisbrecht, B V <br/><br/>
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Jul 1998 
 - 8630-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.95.15.8630  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATPases Associated with Diverse Cellular Activities<br/>Adenosine Triphosphatases--genetics<br/>Adrenoleukodystrophy--genetics<br/>Glycoproteins--genetics<br/>Humans<br/>Infant, Newborn<br/>Membrane Proteins<br/>Peroxisomal Disorders--genetics<br/>Phenotype<br/>Protein Binding