Babilas, P <br/><br/>
Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis.  [electronic resource] 

 -  The British journal of dermatology  Oct 2009 
 - 944-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2009.09237.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyloidosis, Familial--genetics<br/>Female<br/>Humans<br/>Mutation, Missense--genetics<br/>Oncostatin M Receptor beta Subunit--genetics<br/>Pedigree