Bazzi, Hisham <br/><br/>
Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.  [electronic resource] 

 -  The journal of investigative dermatology. Symposium proceedings  Dec 2005 
 - 222-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1087-0024 
<br/><br/><label>Standard No.: </label>10.1111/j.1087-0024.2005.10110.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Chromosomes, Human, Pair 18<br/>DNA Mutational Analysis<br/>Desmogleins--genetics<br/>Desmosomal Cadherins--genetics<br/>Genes, Recessive<br/>Humans<br/>Hypotrichosis--genetics<br/>Mice<br/>Mutation<br/>Pakistan--ethnology<br/>Rats