Keng, W T <br/><br/>
A3243G mitochondrial mutation associated with polymicrogyria.  [electronic resource] 

 -  Developmental medicine and child neurology  Oct 2003 
 - 704-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0012-1622 
<br/><br/><label>Standard No.: </label>10.1017/s0012162203001300  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Brain--abnormalities<br/>Calcinosis--pathology<br/>Child<br/>DNA, Mitochondrial--genetics<br/>Diffusion Magnetic Resonance Imaging<br/>Female<br/>Gene Expression--genetics<br/>Humans<br/>MELAS Syndrome--diagnosis<br/>Phenotype<br/>Point Mutation--genetics<br/>Tomography, X-Ray Computed