Has, Cristina <br/><br/>
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.  [electronic resource] 

 -  Human mutation  Nov 2011 
 - 1204-12 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.21576  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Blister--genetics<br/>Child<br/>Child, Preschool<br/>Epidermolysis Bullosa--genetics<br/>Genetic Association Studies<br/>Humans<br/>Membrane Proteins--genetics<br/>Mutation<br/>Mutation, Missense<br/>Neoplasm Proteins--genetics<br/>Periodontal Diseases--genetics<br/>Phenotype<br/>Photosensitivity Disorders--genetics