Gruber, Robert <br/><br/>
A novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.  [electronic resource] 

 -  Archives of dermatology  Jun 2011 
 - 748-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1538-3652 
<br/><br/><label>Standard No.: </label>10.1001/archdermatol.2011.138  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acitretin--therapeutic use<br/>Adult<br/>Anti-Infective Agents--therapeutic use<br/>Antigens, Ly--genetics<br/>Biopsy<br/>Homozygote<br/>Humans<br/>Keratoderma, Palmoplantar--diagnosis<br/>Keratolytic Agents--therapeutic use<br/>Male<br/>Mutation, Missense<br/>Phenotype<br/>Urokinase-Type Plasminogen Activator--genetics