Hooper, A J <br/><br/>
Familial lipoprotein lipase deficiency caused by known (G188E) and novel (W394X) LPL gene mutations.  [electronic resource] 

 -  Annals of clinical biochemistry  Jan 2008 
 - 102-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0004-5632 
<br/><br/><label>Standard No.: </label>10.1258/acb.2007.007080  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Amino Acids--genetics<br/>Child<br/>Female<br/>Humans<br/>Hyperlipoproteinemia Type I--blood<br/>Lipoprotein Lipase--genetics<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Pedigree