Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes-Reference-Cited by-同舟云学术

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Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes

Published:2018-06 Issue:3 Volume:20 Page:214-218
ISSN:1294-9361
Container-title:Epileptic Disorders
language:
Short-container-title:

Author:

Aravindhan Akilandeswari,Shah Kinal,Pak Jayoung,Veerapandiyan Aravindhan

Publisher

John Libbey Eurotext

Subject

Clinical Neurology,Neurology,General Medicine

Cited by 10 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. Phenotypic Spectrum of STXBP1 Gene Mutations in an Emirati Case Series;Cureus;2023-09-29

2. Sleep architecture in neonatal and infantile onset epilepsies in the first six months of life: A scoping review;European Journal of Paediatric Neurology;2022-11

3. Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes;Frontiers in Neurology;2022-03-11

4. Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery;Frontiers in Neurology;2022-01-13

5. Extending the clinical phenotype of SPTAN1 : From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability;American Journal of Medical Genetics Part A;2021-09-30

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