A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. [electronic resource]
Producer: 19980316Description: 51-61 p. digitalISSN:- 0092-8674
- Adolescent
- Amino Acid Sequence
- Base Sequence
- Cell Movement -- genetics
- Central Nervous System -- metabolism
- Cerebral Cortex -- abnormalities
- Child, Preschool
- Chromosome Mapping
- Chromosomes, Artificial, Yeast
- DNA, Complementary -- analysis
- Doublecortin Domain Proteins
- Epilepsy -- genetics
- Family Health
- Female
- Gene Expression -- genetics
- Genes -- genetics
- Humans
- Male
- Microtubule-Associated Proteins
- Molecular Sequence Data
- Mutation -- genetics
- Neurons -- chemistry
- Neuropeptides -- genetics
- Pedigree
- Peptides -- genetics
- Sequence Homology, Amino Acid
- Sequence Tagged Sites
- Sex Chromosome Aberrations -- genetics
- Syndrome
- Transcription, Genetic -- genetics
- X Chromosome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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