Hobson, G <br/><br/>
A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.  [electronic resource] 

 -  Human mutation  Feb 2001 
 - 152 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/1098-1004(200102)17:2<152::AID-HUMU9>3.0.CO;2-P  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA--genetics<br/>Deoxyribonuclease HpaII--metabolism<br/>Deoxyribonucleases, Type II Site-Specific--metabolism<br/>Genetic Carrier Screening<br/>Humans<br/>Myelin Proteolipid Protein--genetics<br/>Pelizaeus-Merzbacher Disease--genetics<br/>Polymorphism, Genetic<br/>Polymorphism, Restriction Fragment Length