Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits. [electronic resource]
Producer: 20130523Description: 4386-91 p. digitalISSN:- 1091-6490
- Amino Acid Substitution
- Animals
- Anticonvulsants -- pharmacology
- CHO Cells
- Carbamates -- pharmacology
- Cricetinae
- Cricetulus
- Epilepsy, Benign Neonatal -- genetics
- Genotype
- Humans
- KCNQ2 Potassium Channel -- chemistry
- KCNQ3 Potassium Channel -- genetics
- Models, Molecular
- Mutation, Missense
- Phenotype
- Phenylenediamines -- pharmacology
- Pyramidal Cells -- metabolism
- Structural Homology, Protein
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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