Kotze, M J <br/><br/>
Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis.  [electronic resource] 

 -  Molecular and cellular probes  Dec 1994 
 - 513-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0890-8508 
<br/><br/><label>Standard No.: </label>10.1006/mcpr.1994.1072  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Apolipoprotein B-100<br/>Apolipoproteins B--deficiency<br/>Base Sequence<br/>Coronary Disease--genetics<br/>Genes, Dominant--genetics<br/>Genetic Carrier Screening<br/>Humans<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Nucleic Acid Heteroduplexes--isolation & purification<br/>Pedigree<br/>Polymerase Chain Reaction--methods<br/>Receptors, LDL--genetics