Naseer, Muhammad Imran <br/><br/>
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.  [electronic resource] 

 -  Annals of Saudi medicine   
 - 148-153 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0975-4466 
<br/><br/><label>Standard No.: </label>10.5144/0256-4947.2017.148  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Cell Cycle Proteins<br/>Child<br/>Consanguinity<br/>Cross-Sectional Studies<br/>Exome--genetics<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Microcephaly--genetics<br/>Mutation, Missense<br/>Nerve Tissue Proteins--genetics<br/>Saudi Arabia<br/>Young Adult