Sgourdou, Paraskevi <br/><br/>
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.  [electronic resource] 

 -  Scientific reports  03 2017 
 - 43708 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>2045-2322 
<br/><br/><label>Standard No.: </label>10.1038/srep43708  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Aurora Kinase B--genetics<br/>Brain--abnormalities<br/>Cell Cycle--genetics<br/>Cell Cycle Proteins<br/>Cell Differentiation--genetics<br/>Cell Proliferation<br/>Centrosome--metabolism<br/>Consanguinity<br/>Disease Models, Animal<br/>Epistasis, Genetic<br/>Fluorescent Antibody Technique<br/>Gene Expression<br/>Humans<br/>Inheritance Patterns<br/>Male<br/>Mice<br/>Mice, Knockout<br/>Microcephaly--diagnostic imaging<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Neural Stem Cells--metabolism<br/>Pedigree<br/>Whole Genome Sequencing