标题
DEPDC5does it all: Shared genetics for diverse epilepsy syndromes
作者
关键词
-
出版物
ANNALS OF NEUROLOGY
Volume 75, Issue 5, Pages 631-633
出版商
Wiley
发表日期
2014-04-20
DOI
10.1002/ana.24160
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations in mammalian target of rapamycin regulatorDEPDC5cause focal epilepsy with brain malformations
- (2014) Ingrid E. Scheffer et al. ANNALS OF NEUROLOGY
- DEPDC5mutations in genetic focal epilepsies of childhood
- (2014) Dennis Lal et al. ANNALS OF NEUROLOGY
- Familial risk of epilepsy: a population-based study
- (2014) Anna L. Peljto et al. BRAIN
- Rolandic epilepsy has little effect on adult life 30 years later: A population-based study
- (2014) C. S. Camfield et al. NEUROLOGY
- Everolimus treatment of refractory epilepsy in tuberous sclerosis complex
- (2013) Darcy A. Krueger et al. ANNALS OF NEUROLOGY
- A recurrent mutation inDEPDC5predisposes to focal epilepsies in the French-Canadian population
- (2013) C. Martin et al. CLINICAL GENETICS
- A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes includingGRIN2AandPRRT2
- (2013) Sarra Dimassi et al. EPILEPSIA
- Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
- (2013) Johannes R Lemke et al. NATURE GENETICS
- Mutations of DEPDC5 cause autosomal dominant focal epilepsies
- (2013) Saeko Ishida et al. NATURE GENETICS
- Mutations in DEPDC5 cause familial focal epilepsy with variable foci
- (2013) Leanne M Dibbens et al. NATURE GENETICS
- GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
- (2013) Gaetan Lesca et al. NATURE GENETICS
- Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family
- (2013) Veronica Sansoni et al. PLoS One
- RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
- (2013) Dennis Lal et al. PLoS One
- Epi4K: Gene discovery in 4,000 genomes
- (2012) EPILEPSIA
- Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
- (2012) Sarah E Heron et al. NATURE GENETICS
- Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
- (2012) Annapurna Poduri et al. NEURON
- Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers
- (2011) Daiki Miki et al. NATURE GENETICS
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)
- (2009) Lisa J Strug et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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