The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy-Reference-Cited by-同舟云学术

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The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

Published:2007-07-31 Issue:23 Volume:16 Page:2892-2899
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Martin M. S.,Tang B.,Papale L. A.,Yu F. H.,Catterall W. A.,Escayg A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/23/2892/1481148/ddm248.pdf

Cited by 180 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. Insights into clinical phenotypes and treatment responses in a Small cohort of Taiwanese patients with SCN1A variants: A Preliminary study;Pediatrics & Neonatology;2024-08

2. The contribution of Na_V1.6 to the efficacy of voltage‐gated sodium channel inhibitors in wild type and Na_V1.6 gain‐of‐function (GOF) mouse seizure control;British Journal of Pharmacology;2024-06-24

3. Cardiac-Specific Deletion of Scn8a Mitigates Dravet Syndrome-Associated Sudden Death in Adults;JACC: Clinical Electrophysiology;2024-05

4. Late Sodium Current Promotes Ventricular Arrhythmia in Epilepsy-Related Sudden Death;JACC: Clinical Electrophysiology;2024-05

5. SCN1A Polymorphisms and Haplotypes Are Associated With Valproic Acid Treatment Outcomes in Chinese Children With Epilepsy;Pediatric Neurology;2023-09

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