Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Bibliographic Details
Main Authors: Yang, Xiaoling, Zhang, Yuehua, Xu, Xiaojing, Wang, Shuang, Yang, Zhixian, Wu, Ye, Liu, Xiaoyan, Wu, Xiru
Format: Online
Language:English
Published: BioMed Central 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897939/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897939/

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