Cohen, Rony <br/><br/>
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.  [electronic resource] 

 -  Neurogenetics  10 2016 
 - 251-257 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/s10048-016-0491-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--diagnostic imaging<br/>Child<br/>Cutis Laxa--complications<br/>Epilepsies, Myoclonic--complications<br/>Female<br/>Humans<br/>Male<br/>Mutation<br/>Polymicrogyria--complications<br/>Siblings