The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features.

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Bibliographic Details
Title: The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features.
Authors: Liang, Jao-Shwann1, Lin, Li-Ju2, Yang, Ming-Tao1,3, Wang, Jinn-Shyan2, Lu, Jyh-Feng2 049696@mail.fju.edu.tw
Source: Brain & Development. Nov2017, Vol. 39 Issue 10, p877-881. 5p.
Database: Academic Search Ultimate
Description
ISSN:03877604
DOI:10.1016/j.braindev.2017.06.003