Létard, Pascaline <br/><br/>
Autosomal recessive primary microcephaly due to ASPM mutations: An update.  [electronic resource] 

 -  Human mutation  03 2018 
 - 319-332 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.23381  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Cognition<br/>Cohort Studies<br/>Family<br/>Female<br/>Genetic Association Studies<br/>Geography<br/>Humans<br/>Infant<br/>Magnetic Resonance Imaging<br/>Male<br/>Microcephaly--epidemiology<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics