Genotype-phenotype associations in SCN1A-related epilepsies-Reference-Cited by-同舟云学术

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Genotype-phenotype associations in SCN1A-related epilepsies

Published:2011-01-19 Issue:7 Volume:76 Page:594-600
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Zuberi S. M.,Brunklaus A.,Birch R.,Reavey E.,Duncan J.,Forbes G. H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 226 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. Cerebral venous sinus thrombosis and SCN1A, a novel association?;Molecular Biology Reports;2024-08-01

2. A retrospective study of the yield of next‐generation sequencing in the diagnosis of developmental and epileptic encephalopathies and epileptic encephalopathies in 0–12 years aged children at a single tertiary care hospital in South India;Epileptic Disorders;2024-06-24

3. Fine mapping and candidate gene analysis of Dravet syndrome modifier loci on mouse chromosomes 7 and 8;Mammalian Genome;2024-06-11

4. Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina;Journal of Pediatric Epilepsy;2024-05-31

5. SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations;International Journal of Molecular Sciences;2024-05-22

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