Cavallin, Mara <br/><br/>
Recurrent KIF2A mutations are responsible for classic lissencephaly.  [electronic resource] 

 -  Neurogenetics  Apr 2017 
 - 73-79 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1364-6753 
<br/><br/><label>Standard No.: </label>10.1007/s10048-016-0499-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Classical Lissencephalies and Subcortical Band Heterotopias--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Gene Frequency<br/>Humans<br/>Infant<br/>Kinesins--genetics<br/>Lissencephaly--genetics<br/>Male<br/>Mutation, Missense<br/>Polymorphism, Single Nucleotide