Dravet syndrome: a new causative SCN1A mutation?-Reference-Cited by-同舟云学术

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Dravet syndrome: a new causative SCN1A mutation?

Published:2017-03-18 Issue:5 Volume:5 Page:613-615
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Poryo Martin¹,Clasen Oriana²,Oehl-Jaschkowitz Barbara³,Christmann Alexander³,Gortner Ludwig²,Meyer Sascha²⁴

Affiliation:

1. Department of Pediatric Cardiology; Saarland University Hospital; Homburg/Saar Germany

2. Department of Pediatrics and Neonatology; Saarland University Hospital; Homburg/Saar Germany

3. Gemeinschaftspraxis für Humangenetik; Homburg/Saar Germany

4. Department of Pediatric Neurology; Saarland University Hospital; Homburg/Saar Germany

Publisher

Wiley

Subject

General Medicine

Reference19 articles.

1. Channelopathies as a genetic cause of epilepsy;Mulley;Curr. Opin. Neurol.,2003

2. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am. J. Hum. Genet.,2001

3. SCN1A mutations and epilepsy;Mulley;Hum. Mutat.,2005

4. The spectrum of SCN1A-related infantile epileptic encephalopathies;Harkin;Brain,2007

5. Dravet syndrome: new findings - better and more comprehensive treatment?;Keimer;Epileptologie,2013

Cited by 4 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. Genetics of Dravet Syndrome and its Targeted Therapy by Nanomedicine: A Roadmap for Future Treatment of Drug Resistant Seizures;Current Molecular Pharmacology;2023-06

2. The contribution of fenfluramine to the treatment of Dravet syndrome in Spain through Multi-Criteria Decision Analysis;Epilepsy & Behavior;2022-07

3. The study of sodium and potassium channel gene single-nucleotide variation significance in non-mechanical forms of epilepsy;Egyptian Journal of Medical Human Genetics;2021-01-15

4. Epilepsy-Related Voltage-Gated Sodium Channelopathies: A Review;Frontiers in Pharmacology;2020-08-18

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