Savage, D B <br/><br/>
Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene.  [electronic resource] 

 -  Diabetologia  Apr 2004 
 - 753-6 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0012-186X 
<br/><br/><label>Standard No.: </label>10.1007/s00125-004-1360-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Female<br/>Heterozygote<br/>Humans<br/>Lamin Type A<br/>Lamins--genetics<br/>Lipodystrophy--complications<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Mutation--physiology