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Deep Blue "Seq": Fishing for Epilepsy Genes.Monoaminergic Mechanisms in Epilepsy May Offer Innovative Therapeutic Opportunity for Monoaminergic Multi-Target DrugsGenetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.Integrated network analysis reveals potentially novel molecular mechanisms and therapeutic targets of refractory epilepsies.Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.Genetic risk factors for spontaneous intracerebral haemorrhage.The Epilepsy Spectrum: Targeting Future Research Challenges.Gene-environment interactions in cortical interneuron development and dysfunction: A review of preclinical studies.Childhood epilepsies: What should a pediatrician know?Pore-Forming Proteins as Mediators of Novel Epigenetic Mechanism of Epilepsy.The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.The Cacna1h mutation in the GAERS model of absence epilepsy enhances T-type Ca2+ currents by altering calnexin-dependent trafficking of Cav3.2 channels.Heterozygous STXBP1 Mutations Associated With Ohtahara Syndrome: Two Littles Make a Lot.Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathy.Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy.Does sleep benefit memory consolidation in children with focal epilepsy?GABA type a receptor trafficking and the architecture of synaptic inhibition.Comparison and optimization of in silico algorithms for predicting the pathogenicity of sodium channel variants in epilepsy.Errant gardeners: glial-cell-dependent synaptic pruning and neurodevelopmental disorders.Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.Copy number variation in a hospital-based cohort of children with epilepsy.De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy.Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?Chromatin Remodeling Proteins in Epilepsy: Lessons From CHD2-Associated Epilepsy.Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future
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P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Advancing epilepsy genetics in the genomic era
@ast
Advancing epilepsy genetics in the genomic era
@en
Advancing epilepsy genetics in the genomic era
@nl
type
label
Advancing epilepsy genetics in the genomic era
@ast
Advancing epilepsy genetics in the genomic era
@en
Advancing epilepsy genetics in the genomic era
@nl
prefLabel
Advancing epilepsy genetics in the genomic era
@ast
Advancing epilepsy genetics in the genomic era
@en
Advancing epilepsy genetics in the genomic era
@nl
P2860
P3181
P1433
P1476
Advancing epilepsy genetics in the genomic era
@en
P2093
Candace T Myers
Heather C Mefford
P2860
P2888
P3181
P356
10.1186/S13073-015-0214-7
P407
P5008
P577
2015-08-25T00:00:00Z
P5875
P6179
1015857464