标题
Molecular genetics of Dravet syndrome
作者
关键词
-
出版物
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
Volume 53, Issue -, Pages 7-10
出版商
Wiley
发表日期
2011-04-19
DOI
10.1111/j.1469-8749.2011.03965.x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Sodium channel SCN1A and epilepsy: Mutations and mechanisms
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- Protocadherin 19 mutations in girls with infantile-onset epilepsy
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- Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations
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- A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome
- (2009) Nanda A. Singh et al. PLoS Genetics
- Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
- (2009) Christel Depienne et al. PLoS Genetics
- A catalog of SCN1A variants
- (2008) Christoph Lossin BRAIN & DEVELOPMENT
- Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
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- Inherited Neuronal Ion Channelopathies: New Windows on Complex Neurological Diseases
- (2008) W. A. Catterall et al. JOURNAL OF NEUROSCIENCE
- X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
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