Theart, L <br/><br/>
Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation.  [electronic resource] 

 -  Journal of medical genetics  May 1995 
 - 379-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.32.5.379  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Amino Acid Sequence<br/>Base Sequence<br/>DNA Probes<br/>Exons<br/>Female<br/>Genes, Dominant--genetics<br/>Genotype<br/>Humans<br/>Hyperlipoproteinemia Type II--genetics<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation<br/>New Zealand<br/>Nucleic Acid Heteroduplexes<br/>Receptors, LDL--chemistry<br/>Sequence Deletion