Samanta, Debopam <br/><br/>
Contactin-associated protein-like (CNTNAP) 2 gene mutation in a patient with bilateral schizencephaly.  [electronic resource] 

 -  Acta neurologica Belgica  03 2017 
 - 403-404 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2240-2993 
<br/><br/><label>Standard No.: </label>10.1007/s13760-016-0653-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--diagnostic imaging<br/>Humans<br/>Infant<br/>Magnetic Resonance Imaging<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Schizencephaly--diagnostic imaging