John, Peter <br/><br/>
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.  [electronic resource] 

 -  Archives of dermatological research  Aug 2006 
 - 135-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-3696 
<br/><br/><label>Standard No.: </label>10.1007/s00403-006-0671-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Desmogleins--genetics<br/>Female<br/>Genes, Recessive<br/>Humans<br/>Hypotrichosis--genetics<br/>Male<br/>Pakistan<br/>Pedigree<br/>Sequence Deletion