de Nijs, Laurence <br/><br/>
Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development.  [electronic resource] 

 -  Human molecular genetics  Dec 2012 
 - 5106-17 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/dds356  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Brain--embryology<br/>Calcium-Binding Proteins--genetics<br/>Cell Cycle--genetics<br/>Cell Line<br/>Cell Movement--genetics<br/>Cell Proliferation<br/>Humans<br/>Intracellular Space--metabolism<br/>Mice<br/>Mutation<br/>Myoclonic Epilepsy, Juvenile--embryology<br/>Neuroglia--metabolism<br/>Neurons--metabolism<br/>Protein Transport<br/>Rats<br/>Spindle Apparatus--genetics<br/>Stem Cells--metabolism