SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis

Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic encephalopathy. More than 1,800 mutations have been identified in SCN1A. Although it is known that SCN1A is the main cause of DS and...

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Detalles Bibliográficos
Autores principales: Ding, Jiangwei, Li, Xinxiao, Tian, Haiyan, Wang, Lei, Guo, Baorui, Wang, Yangyang, Li, Wenchao, Wang, Feng, Sun, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739186/
https://www.ncbi.nlm.nih.gov/pubmed/35002916
http://dx.doi.org/10.3389/fneur.2021.743726

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739186/
https://www.ncbi.nlm.nih.gov/pubmed/35002916
http://dx.doi.org/10.3389/fneur.2021.743726

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