A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: Is there a common core deficit?

出版年份 2015 全文链接

标题

作者

关键词

SCN1A, gene, Dravet syndrome spectrum, Neuropsychological phenotype

出版物

Volume 43, Issue -, Pages 89-92

出版商

Elsevier BV

发表日期

2015-01-07

DOI

10.1016/j.yebeh.2014.11.009

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