Larsen, Jan <br/><br/>
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.  [electronic resource] 

 -  Epilepsia  Dec 2015 
 - e203-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-1167 
<br/><br/><label>Standard No.: </label>10.1111/epi.13222  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carbohydrate Metabolism, Inborn Errors--epidemiology<br/>Child, Preschool<br/>Denmark--epidemiology<br/>Epilepsies, Myoclonic--genetics<br/>Epilepsy, Absence--genetics<br/>Epilepsy, Generalized--genetics<br/>Glucose Transporter Type 1--deficiency<br/>Humans<br/>Infant<br/>Monosaccharide Transport Proteins--deficiency<br/>Mutation<br/>Syndrome