Kremer, H <br/><br/>
An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1.  [electronic resource] 

 -  The Journal of investigative dermatology  Dec 1998 
 - 1224-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-202X 
<br/><br/><label>Standard No.: </label>10.1046/j.1523-1747.1998.00389.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Genetic Linkage--genetics<br/>Humans<br/>Hyperkeratosis, Epidermolytic--genetics<br/>Keratins--chemistry<br/>Lod Score<br/>Microscopy, Electron<br/>Mutation<br/>Pedigree<br/>Protein Structure, Tertiary