Yum, Mi-Sun <br/><br/>
The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.  [electronic resource] 

 -  Journal of Korean medical science  Feb 2010 
 - 324-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1598-6357 
<br/><br/><label>Standard No.: </label>10.3346/jkms.2010.25.2.324  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Electroencephalography<br/>Epilepsy, Benign Neonatal--diagnosis<br/>Female<br/>Humans<br/>Infant, Newborn<br/>KCNQ2 Potassium Channel--genetics<br/>Magnetic Resonance Imaging<br/>Mutation<br/>Pedigree<br/>Republic of Korea<br/>Sequence Analysis, DNA