Mochida, Ganeshwaran H <br/><br/>
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.  [electronic resource] 

 -  American journal of human genetics  Dec 2010 
 - 882-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2010.10.026  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Calcinosis--genetics<br/>Cataract--congenital<br/>Cell Adhesion Molecules--genetics<br/>Cerebral Hemorrhage--genetics<br/>Child<br/>Ependyma--pathology<br/>Female<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Pedigree<br/>Tight Junctions--metabolism