research article
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of Kv7.2 potassium channel subunits
Abstract
Abstract is not available.- info:eu-repo/semantics/article
- Anticonvulsant
- Brain development
- Channelopathie
- P-stacking interaction
- Potassium channel gating
- Amino Acid Substitution
- Animal
- Anticonvulsant
- CHO Cell
- Carbamate
- Cricetinae
- Cricetulu
- Epilepsy, Benign Neonatal
- Genotype
- Human
- KCNQ2 Potassium Channel
- KCNQ3 Potassium Channel
- Models, Molecular
- Phenotype
- Phenylenediamine
- Pyramidal Cell
- Structural Homology, Protein
- Mutation, Missense
- Multidisciplinary
Similar works
Full text
Last time updated on 08/02/2017
This paper was published in Archivio della ricerca - Università degli studi di Napoli Federico II.
Having an issue?
Is data on this page outdated, violates copyrights or anything else? Report the problem now and we will take corresponding actions after reviewing your request.
Licence: license uri:http://creativecommons.org/publicdomain/zero/1.0/