Li, M <br/><br/>
Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease.  [electronic resource] 

 -  The British journal of dermatology  Mar 2016 
 - 663-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/bjd.14178  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Exome--genetics<br/>Genetic Linkage--genetics<br/>Humans<br/>Hyperpigmentation--genetics<br/>Keratin-5--genetics<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Pigmentation Disorders--congenital<br/>Skin Diseases, Genetic--genetics<br/>Skin Diseases, Papulosquamous--genetics