Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. [electronic resource]
Producer: 20150817Description: 992-1000 p. digitalISSN:- 1537-6605
- Animals
- Base Sequence
- Cell Adhesion Molecules, Neuronal -- blood
- Chromosome Mapping
- Epilepsy, Frontal Lobe -- genetics
- Exome
- Extracellular Matrix Proteins -- blood
- Fluorescent Antibody Technique
- Gene Components
- Humans
- Immunoblotting
- Intercellular Signaling Peptides and Proteins
- Models, Molecular
- Molecular Sequence Data
- Mutation, Missense -- genetics
- Nerve Tissue Proteins -- blood
- Pedigree
- Polymorphism, Single Nucleotide -- genetics
- Protein Conformation
- Protein Folding
- Proteins -- metabolism
- Rats
- Reelin Protein
- Sequence Analysis, DNA
- Serine Endopeptidases -- blood
- Sleep Wake Disorders -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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