Fertig, Evan <br/><br/>
Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.  [electronic resource] 

 -  Neurology  May 2003 
 - 1687-90 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000063324.39980.4a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Aged, 80 and over<br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Auditory Perceptual Disorders--genetics<br/>Chromosomes, Human, Pair 10--genetics<br/>DNA Mutational Analysis<br/>Epilepsy, Temporal Lobe--genetics<br/>Exons--genetics<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Intracellular Signaling Peptides and Proteins<br/>Italy<br/>Male<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Point Mutation<br/>Protein Structure, Tertiary<br/>Proteins--genetics<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Tinnitus--genetics