Kudin, Alexei P <br/><br/>
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.  [electronic resource] 

 -  Free radical biology & medicine  05 2017 
 - 270-277 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1873-4596 
<br/><br/><label>Standard No.: </label>10.1016/j.freeradbiomed.2017.02.040  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Epilepsy, Generalized--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Glutathione--metabolism<br/>Homozygote<br/>Humans<br/>Male<br/>Muscle, Skeletal--metabolism<br/>Mutation<br/>Oxidative Stress--genetics<br/>Reactive Oxygen Species--metabolism<br/>Thioredoxin Reductase 1--genetics<br/>Exome Sequencing