Issa, Yasmin A <br/><br/>
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.  [electronic resource] 

 -  European journal of human genetics : EJHG  10 2016 
 - 1430-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2016.29  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Anodontia--diagnosis<br/>Child<br/>Chromosomes, Human, Pair 22--genetics<br/>Ectodermal Dysplasia--diagnosis<br/>Exome<br/>Female<br/>Genes, Recessive<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation<br/>Pedigree<br/>Syndrome<br/>Wnt Signaling Pathway