Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsy
about
Models for discovery of targeted therapy in genetic epileptic encephalopathies.Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation.Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.Defects at the crossroads of GABAergic signaling in generalized genetic epilepsies.Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2+/Q390X Dravet syndrome mice.SYT1-associated neurodevelopmental disorder: a case series
P2860
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P2860
Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsy
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Differential molecular and beh ...... associated with human epilepsy
@en
Differential molecular and beh ...... ssociated with human epilepsy.
@nl
type
label
Differential molecular and beh ...... associated with human epilepsy
@en
Differential molecular and beh ...... ssociated with human epilepsy.
@nl
prefLabel
Differential molecular and beh ...... associated with human epilepsy
@en
Differential molecular and beh ...... ssociated with human epilepsy.
@nl
P2093
P2860
P356
P1476
Differential molecular and beh ...... associated with human epilepsy
@en
P2093
Jing-Qiong Kang
Robert L Macdonald
Timothy A Warner
Wangzhen Shen
Xuan Huang
P2860
P304
P356
10.1093/HMG/DDW168
P577
2016-06-23T00:00:00Z