Chang, C C <br/><br/>
Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.  [electronic resource] 

 -  American journal of human genetics  Nov 1998 
 - 1294-306 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/302103  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Cell Line<br/>Cells, Cultured<br/>Fibroblasts--metabolism<br/>Genetic Complementation Test<br/>Genotype<br/>Humans<br/>Introns<br/>Membrane Proteins--biosynthesis<br/>Molecular Sequence Data<br/>Oligodeoxyribonucleotides<br/>Open Reading Frames<br/>Peroxisomal Disorders--genetics<br/>Phenotype<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Random Amplified Polymorphic DNA Technique<br/>Recombinant Proteins--biosynthesis<br/>Transfection