Clinical review of genetic epileptic encephalopathies

Clinical review of genetic epileptic encephalopathies

Item
http://www.wikidata.org/entity/Q30537230
Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosumFunctional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.Models for discovery of targeted therapy in genetic epileptic encephalopathies.Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression.GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.Proteomic change by Korean Red Ginseng in the substantia nigra of a Parkinson's disease mouse modelWhole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy
P2860

Clinical review of genetic epileptic encephalopathies

Item
http://www.wikidata.org/entity/Q30537230
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Clinical review of genetic epileptic encephalopathies
@ast
Clinical review of genetic epileptic encephalopathies
@en
type
label
Clinical review of genetic epileptic encephalopathies
@ast
Clinical review of genetic epileptic encephalopathies
@en
prefLabel
Clinical review of genetic epileptic encephalopathies
@ast
Clinical review of genetic epileptic encephalopathies
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P5875
P698
P932
P356
P1433
P1476
Clinical review of genetic epileptic encephalopathies
@en
P2093
P2860
P304
P31
P356
10.1016/J.EJMG.2011.12.010
P433
P478
P577
P5875
P698
P932