The variable phenotypes of KCNQ-related epilepsy. [electronic resource]
Producer: 20141103Description: e99-105 p. digitalISSN:- 1528-1167
- Basal Ganglia -- pathology
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- Electroencephalography
- Epilepsy -- genetics
- Female
- Genetic Association Studies
- Humans
- Infant
- Infant, Newborn
- KCNQ Potassium Channels -- genetics
- Magnetic Resonance Imaging
- Male
- Mutation -- genetics
- Phenotype
- Thalamus -- pathology
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Publication Type: Journal Article
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