Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features. [electronic resource]
Producer: 20040129Description: 1687-90 p. digitalISSN:- 1526-632X
- Aged
- Aged, 80 and over
- Amino Acid Sequence
- Amino Acid Substitution
- Auditory Perceptual Disorders -- genetics
- Chromosomes, Human, Pair 10 -- genetics
- DNA Mutational Analysis
- Epilepsy, Temporal Lobe -- genetics
- Exons -- genetics
- Female
- Genes, Dominant
- Humans
- Intracellular Signaling Peptides and Proteins
- Italy
- Male
- Molecular Sequence Data
- Mutation, Missense
- Pedigree
- Point Mutation
- Protein Structure, Tertiary
- Proteins -- genetics
- Sequence Alignment
- Sequence Homology, Amino Acid
- Tinnitus -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.