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Title
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy
Authors
Keywords
Early-onset epilepsy, Whole-exome sequencing, <em class="EmphasisTypeItalic ">SETD1A</em>, Neural development
Journal
Neuroscience Bulletin
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2019-06-14
DOI
10.1007/s12264-019-00400-w
References
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Related references
Note: Only part of the references are listed.- Clinical and genetic spectrum of a large cohort of children with epilepsy in China
- (2018) Lin Yang et al. GENETICS IN MEDICINE
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- (2018) Peter L. Hsu et al. CELL
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- (2018) Qianhui Qu et al. CELL
- RNF8/UBC13 ubiquitin signaling suppresses synapse formation in the mammalian brain
- (2017) Pamela Valnegri et al. Nature Communications
- A Road Map for Precision Cancer Medicine Using Personalized Models
- (2017) Gabriele Picco et al. Cancer Discovery
- The genetic landscape of the epileptic encephalopathies of infancy and childhood
- (2016) Amy McTague et al. LANCET NEUROLOGY
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
- (2016) Tarjinder Singh et al. NATURE NEUROSCIENCE
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
- (2015) Stephan J. Sanders et al. NEURON
- Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes
- (2015) Mario Mastrangelo PEDIATRIC NEUROLOGY
- Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene
- (2014) Atsushi Takata et al. NEURON
- The n-SET Domain of Set1 Regulates H2B Ubiquitylation-Dependent H3K4 Methylation
- (2013) Jaehoon Kim et al. MOLECULAR CELL
- Extending the KCNQ2 encephalopathy spectrum: Clinical and neuroimaging findings in 17 patients
- (2013) S. Weckhuysen et al. NEUROLOGY
- The COMPASS Family of Histone H3K4 Methylases: Mechanisms of Regulation in Development and Disease Pathogenesis
- (2012) Ali Shilatifard Annual Review of Biochemistry
- A population-based study of newly diagnosed epilepsy in infants
- (2012) Christin M. Eltze et al. EPILEPSIA
- Targeted next generation sequencing as a diagnostic tool in epileptic disorders
- (2012) Johannes R. Lemke et al. EPILEPSIA
- Genetics of epilepsy syndromes starting in the first year of life
- (2009) L. Deprez et al. NEUROLOGY
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