Okumoto, K <br/><br/>
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.  [electronic resource] 

 -  Molecular and cellular biology  Jul 1998 
 - 4324-36 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0270-7306 
<br/><br/><label>Standard No.: </label>10.1128/MCB.18.7.4324  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>CHO Cells<br/>Cell Line<br/>Cell Line, Transformed<br/>Cloning, Molecular<br/>Cricetinae<br/>Cytosol<br/>DNA, Complementary<br/>Fibroblasts<br/>Humans<br/>Membrane Proteins--genetics<br/>Microbodies--metabolism<br/>Molecular Sequence Data<br/>Mutagenesis<br/>Mutation<br/>Peroxisomal Disorders--veterinary<br/>Rats<br/>Sequence Homology, Amino Acid<br/>Zellweger Syndrome--genetics<br/>Zinc Fingers