TY  - GEN
AU  - Fertig,Evan
AU  - Lincoln,Anne
AU  - Martinuzzi,Andrea
AU  - Mattson,Richard H
AU  - Hisama,Fuki M
TI  - Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features
SN  - 1526-632X
PY  - 2004///0129
KW  - Aged
KW  - Aged, 80 and over
KW  - Amino Acid Sequence
KW  - Amino Acid Substitution
KW  - Auditory Perceptual Disorders
KW  - genetics
KW  - Chromosomes, Human, Pair 10
KW  - DNA Mutational Analysis
KW  - Epilepsy, Temporal Lobe
KW  - Exons
KW  - Female
KW  - Genes, Dominant
KW  - Humans
KW  - Intracellular Signaling Peptides and Proteins
KW  - Italy
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Pedigree
KW  - Point Mutation
KW  - Protein Structure, Tertiary
KW  - Proteins
KW  - Sequence Alignment
KW  - Sequence Homology, Amino Acid
KW  - Tinnitus
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/01.wnl.0000063324.39980.4a
ER  -