Pérez-Aguilar, Fernando <br/><br/>
Aceruloplasminemia in an asymptomatic patient with a new mutation. Diagnosis and family genetic analysis.  [electronic resource] 

 -  Journal of hepatology  Jun 2005 
 - 947-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0168-8278 
<br/><br/><label>Standard No.: </label>10.1016/j.jhep.2005.02.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brain--pathology<br/>Ceruloplasmin--genetics<br/>Ferritins--blood<br/>Hepatocytes--metabolism<br/>Humans<br/>Iron--metabolism<br/>Iron Overload--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Mutation, Missense<br/>Pedigree