Miceli, Francesco <br/><br/>
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Mar 2013 
 - 4386-91 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1091-6490 
<br/><br/><label>Standard No.: </label>10.1073/pnas.1216867110  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Animals<br/>Anticonvulsants--pharmacology<br/>CHO Cells<br/>Carbamates--pharmacology<br/>Cricetinae<br/>Cricetulus<br/>Epilepsy, Benign Neonatal--genetics<br/>Genotype<br/>Humans<br/>KCNQ2 Potassium Channel--chemistry<br/>KCNQ3 Potassium Channel--genetics<br/>Models, Molecular<br/>Mutation, Missense<br/>Phenotype<br/>Phenylenediamines--pharmacology<br/>Pyramidal Cells--metabolism<br/>Structural Homology, Protein