García, M <br/><br/>
Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.  [electronic resource] 

 -  The British journal of dermatology  Sep 2011 
 - 683-92 p.  digital 
<br/><br/> Publication Type: 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.1365-2133.2011.10428.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child, Preschool<br/>Cohort Studies<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Epidermolysis Bullosa Simplex--genetics<br/>Female<br/>Homozygote<br/>Humans<br/>Infant<br/>Keratin-14--genetics<br/>Keratin-5--genetics<br/>Male<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Spain<br/>Young Adult