A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
about
Potassium Channels and Human Epileptic Phenotypes: An Updated OverviewAn integer programming framework for inferring disease complexes from network data.Novel genetic causes for cerebral visual impairmentRetigabine holds KV7 channels open and stabilizes the resting potential.Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures.Involvement of cortical fast-spiking parvalbumin-positive basket cells in epilepsy.Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.Potassium Channels in Epilepsy.Hysteresis in voltage-gated channelsCalmodulin regulates KCNQ2 function in epilepsy.Models for discovery of targeted therapy in genetic epileptic encephalopathies.The anticonvulsant retigabine suppresses neuronal KV2-mediated currents.Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy.Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.Recent Advances in Neonatal Seizures.
P2860
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P2860
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
A novel KCNQ3 mutation in fami ...... s and intellectual disability.
@en
type
label
A novel KCNQ3 mutation in fami ...... s and intellectual disability.
@en
prefLabel
A novel KCNQ3 mutation in fami ...... s and intellectual disability.
@en
P2093
P2860
P50
P356
P1433
P1476
A novel KCNQ3 mutation in fami ...... s and intellectual disability.
@en
P2093
Angela Robbiano
Antonina Fontana
Giulia Bellini
Pasquale Striano
Rosaria Nardello
Salvatore Mangano
P2860
P304
P356
10.1111/EPI.12887
P577
2014-12-19T00:00:00Z