Data on mutations and Clinical features in SCN1A or SCN2A gene

Mutations in SCN1A and SCN2A are associated with a wide spectrum of epilepsy related disorders in human. This dataset presented variants and clinical features of SCN1A and SCN2A genes. A total of 48 cases were presented, including 33 SCN1A mutations and 14 SCN2A mutations. While 22 mutations were no...

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Detalles Bibliográficos
Autores principales: Kong, Yanting, Yan, Kai, Hu, Liyuan, Wang, Mingbang, Dong, Xinran, Lu, Yulan, Wu, Bingbing, Wang, Huijun, Yang, Lin, Zhou, Wenhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Physics and Astronomy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314000/
https://www.ncbi.nlm.nih.gov/pubmed/30619928
http://dx.doi.org/10.1016/j.dib.2018.08.122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314000/
https://www.ncbi.nlm.nih.gov/pubmed/30619928
http://dx.doi.org/10.1016/j.dib.2018.08.122

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