Kozusko, K <br/><br/>
Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophy.  [electronic resource] 

 -  Diabetes  Jan 2015 
 - 299-310 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1939-327X 
<br/><br/><label>Standard No.: </label>10.2337/db14-0104  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>1-Acylglycerol-3-Phosphate O-Acyltransferase--metabolism<br/>3T3-L1 Cells<br/>Adipocytes, White--physiology<br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>Diabetes Mellitus, Type 2--genetics<br/>Family Health<br/>Female<br/>Frameshift Mutation<br/>Humans<br/>Hyperlipoproteinemia Type IV--genetics<br/>Insulin Resistance--genetics<br/>Lipodystrophy, Familial Partial--genetics<br/>Male<br/>Mice<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Pedigree<br/>Perilipin-1<br/>Phosphoproteins--genetics