Chen, Yucai <br/><br/>
Association between genetic variation of CACNA1H and childhood absence epilepsy.  [electronic resource] 

 -  Annals of neurology  Aug 2003 
 - 239-43 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.10607  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Amino Acid Substitution<br/>Calcium Channels, T-Type--genetics<br/>Child<br/>Child, Preschool<br/>China<br/>DNA--genetics<br/>Electroencephalography<br/>Epilepsy, Absence--genetics<br/>Exons--genetics<br/>Female<br/>Genetic Variation<br/>Humans<br/>Male<br/>Mutation, Missense--genetics<br/>Reverse Transcriptase Polymerase Chain Reaction