Takizawa, Y <br/><br/>
Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing.  [electronic resource] 

 -  The Journal of investigative dermatology  Dec 1998 
 - 1239-41 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-202X 
<br/><br/><label>Standard No.: </label>10.1038/sj.jid.5600370  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Codon, Nonsense--genetics<br/>Epidermolysis Bullosa, Junctional--epidemiology<br/>Frameshift Mutation<br/>Humans<br/>Japan--epidemiology<br/>Laminin--genetics<br/>Mutation<br/>Prenatal Diagnosis