Mirzaa, Ghayda M <br/><br/>
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.  [electronic resource] 

 -  The Lancet. Neurology  Dec 2015 
 - 1182-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1474-4465 
<br/><br/><label>Standard No.: </label>10.1016/S1474-4422(15)00278-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Malformations of Cortical Development--genetics<br/>Mutation<br/>Phosphatidylinositol 3-Kinases--genetics<br/>Young Adult