Pulkkinen, L <br/><br/>
Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia.  [electronic resource] 

 -  Human molecular genetics  May 1997 
 - 669-74 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/6.5.669  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antigens, CD--genetics<br/>Blister<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 2<br/>Duodenal Obstruction--congenital<br/>Epidermolysis Bullosa, Junctional--complications<br/>Exons<br/>Female<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Integrin alpha6<br/>Introns<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Pregnancy