Genetically complex epilepsies, copy number variants and syndrome constellations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine
Cited by 33 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
1. Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing—A Multicenter Cohort Study;Pediatric Neurology;2024-10
2. An Experimental Evaluation of Anticonvulsant Activity of Ethanolic Extract of <i>Vitex negundo</i> Linn. on Validated Animal Model;International Journal of Newgen Research in Pharmacy & Healthcare;2024-06-30
3. Knowledge about the Management of Anti-Epileptic Drug Treatment among General Practitioners in Brazzaville, Congo;Neuroscience and Medicine;2023
4. Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosis;PLOS ONE;2021-09-01
5. ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder;Clinical Genetics;2021-07-16
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