Christiano, A M <br/><br/>
Genetic basis of Bart's syndrome: a glycine substitution mutation in the type VII collagen gene.  [electronic resource] 

 -  The Journal of investigative dermatology  Jun 1996 
 - 1340-2 p.  digital 
<br/><br/> Publication Type: Corrected and Republished Article; Journal Article; 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>10.1111/1523-1747.ep12349293  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Collagen--genetics<br/>Epidermolysis Bullosa Dystrophica--genetics<br/>Glycine<br/>Humans<br/>Mutation<br/>Nucleic Acid Heteroduplexes<br/>Pedigree<br/>Polymerase Chain Reaction