Shimomura, Yutaka <br/><br/>
Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.  [electronic resource] 

 -  Experimental dermatology  Mar 2009 
 - 218-21 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1600-0625 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0625.2008.00788.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Case-Control Studies<br/>Child<br/>Female<br/>Hair--pathology<br/>Homozygote<br/>Humans<br/>Hypotrichosis--ethnology<br/>Iran<br/>Lipase--metabolism<br/>Lysophospholipids--metabolism<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Receptors, Purinergic P2--analysis<br/>Signal Transduction--physiology