Drévillon, Loïc <br/><br/>
KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome.  [electronic resource] 

 -  Human molecular genetics  Jun 2013 
 - 2387-99 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddt083  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Actins--genetics<br/>Adolescent<br/>Adult<br/>Child<br/>Craniofacial Abnormalities--genetics<br/>Female<br/>France<br/>Hirschsprung Disease--genetics<br/>Humans<br/>Infant<br/>Iraq<br/>Male<br/>Microtubules--genetics<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Pedigree<br/>Protein Binding<br/>Tubulin--genetics<br/>White People--genetics