van Steensel, M A M <br/><br/>
A missense mutation in KRT14 causing a dermatopathia pigmentosa reticularis/Naegeli-Franceschetti-Jadassohn phenotype.  [electronic resource] 

 -  Journal of the European Academy of Dermatology and Venereology : JEADV  Sep 2010 
 - 1116-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-3083 
<br/><br/><label>Standard No.: </label>10.1111/j.1468-3083.2010.03598.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Female<br/>Humans<br/>Hyperpigmentation--genetics<br/>Mutation, Missense<br/>Phenotype