Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain. [electronic resource]
Producer: 20090825Description: 173-93 p. digitalISSN:- 1432-1203
- ADAM Proteins -- genetics
- ADAMTS4 Protein
- Brain -- anatomy & histology
- Cathepsin B -- genetics
- Cerebral Cortex -- abnormalities
- Child, Preschool
- Chromosomes, Human, Pair 16
- Chromosomes, Human, Pair 22
- Chromosomes, Human, Pair 3
- Classical Lissencephalies and Subcortical Band Heterotopias -- complications
- Collagen Type XVIII
- Epilepsy -- etiology
- Eye Proteins -- genetics
- Homeodomain Proteins -- genetics
- Humans
- Lissencephaly -- complications
- Male
- Malformations of Cortical Development -- complications
- Membrane Proteins
- Mutation
- Neoplasm Proteins
- Nerve Tissue Proteins -- genetics
- PAX6 Transcription Factor
- Paired Box Transcription Factors -- genetics
- Periventricular Nodular Heterotopia -- complications
- Procollagen N-Endopeptidase -- genetics
- Radiography
- Receptors, G-Protein-Coupled -- genetics
- Repressor Proteins -- genetics
- T-Box Domain Proteins -- genetics
- Transcription Factors -- genetics
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Publication Type: Comparative Study; Journal Article; Review
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