Funder
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
U.S. Department of Health & Human Services | NIH | National Cancer Institute
U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences
U.S. Department of Health & Human Services | National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference58 articles.
1. Gaily, E., Lommi, M., Lapatto, R. & Lehesjoki, A.-E. Incidence and outcome of epilepsy syndromes with onset in the first year of life: a retrospective population-based study. Epilepsia 57, 1594–1601 (2016).
2. OHTAHARA, S. On the specific age-dependent epileptic syndrome: the early-infantile epileptic encephalopathy with suppression-burst. No To Hattatsu 8, 271–279 (1976).
3. Nordli, D. R. Jr. Epileptic encephalopathies in infants and children. J. Clin. Neurophysiol. 29, 420–424 (2012).
4. Berg, A. T. et al. Early-life epilepsies and the emerging role of genetic testing. JAMA Pediatr. 171, 863–871 (2017).
5. Allen, N. M. et al. Chromosomal microarray in unexplained severe early onset epilepsy—a single centre cohort. Eur. J. Paediatr. Neurol. 19, 390–394 (2015).
Cited by
69 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献