Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy. [electronic resource]
Producer: 20170515Description: 1975-1984 p. digitalISSN:- 1526-632X
- Aged
- Animals
- Anticonvulsants -- therapeutic use
- Ataxia -- genetics
- Child
- Child, Preschool
- Cohort Studies
- DNA Mutational Analysis
- Epilepsy -- drug therapy
- Family Health
- Female
- Humans
- Infant
- Kv1.2 Potassium Channel -- genetics
- Male
- Membrane Potentials -- genetics
- Middle Aged
- Models, Chemical
- Mutation -- genetics
- Oocytes
- Pharmacogenetics
- Xenopus laevis
- Young Adult
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Publication Type: Journal Article
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