Martignago, B C F <br/><br/>
Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.  [electronic resource] 

 -  The British journal of dermatology  Dec 2007 
 - 1281-4 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-0963 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2007.08219.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Genetic Carrier Screening<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Neoplasm Proteins--genetics<br/>Pedigree<br/>Skin Diseases, Genetic--genetics<br/>Syndrome