Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
about
BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsyHuman gamma-aminobutyric acid type B receptors are differentially expressed and regulate inwardly rectifying K+ channelsAdvances in genetics of juvenile myoclonic epilepsiesIon channels and epilepsyMutations in EFHC1 cause juvenile myoclonic epilepsyIdiopathic epilepsies with a complex mode of inheritance.Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.GABAergic neuron deficit as an idiopathic generalized epilepsy mechanism: the role of BRD2 haploinsufficiency in juvenile myoclonic epilepsy.Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsySex-specific behavioral traits in the Brd2 mouse model of juvenile myoclonic epilepsyJuvenile myoclonic epilepsy: under-appreciated and under-diagnosedComplex inheritance and parent-of-origin effect in juvenile myoclonic epilepsyGenetics of inherited human epilepsiesRecent developments in the quest for myoclonic epilepsy genes.The state of the art in the genetic analysis of the epilepsiesSeizures of idiopathic generalized epilepsies.Evaluating candidate genes in common epilepsies and the nature of evidenceGenetic association analysis: a primer on how it works, its strengths and its weaknesses.Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.Double bromodomain-containing gene Brd2 is essential for embryonic development in mouseGenetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain.Genetic evaluation and counseling for epilepsy.Susceptibility Gene for Juvenile Myoclonic Epilepsy Rings True.Association analysis of BRD2 (RING3) and epilepsy in a Dutch population.A locus for juvenile myoclonic epilepsy maps to 2q33-q36.Neuropsychological EEG activation in patients with epilepsy.Exploration of the genetic architecture of idiopathic generalized epilepsies.A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic EpilepsyILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies
P2860
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P2860
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
description
1997 nî lūn-bûn
@nan
1997 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@ast
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@en
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@nl
type
label
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@ast
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@en
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@nl
prefLabel
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@ast
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@en
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@nl
P2093
P356
P1433
P1476
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
@en
P2093
Beck-Mannagetta G
Blasczyk R
Bockenkamp B
Hildmann T
P304
P356
10.1212/WNL.49.3.842
P407
P577
1997-09-01T00:00:00Z