Analysis of the CHRNA7 gene mutation and polymorphism in Southern Han Chinese patients with nocturnal frontal epilepsy

Objective:To detect the CHRNA7 gene mutation and polymorphism in Southern Han Chinese patients with nocturnal frontal lobe epilepsy(NFLE).Methods:Blood samples were collected from 215 Southern Han Chinese patients with NFLE and 200 healthy Southern Han Chinese control subjects.Genomic DNA was extrac...

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Veröffentlicht in:	Asian Pacific journal of tropical medicine 2015-04, Vol.8 (4), p.330-333
Hauptverfasser:	Chen, Zhi-Hong, Wang, Chun, Wang, Lin-Gan, Zhuo, Mu-Qing, Tang, Zhi-Hong, Zhai, Qiong-Xiang, Chen, Qian, Guo, Yu-Xiong, Zhang, Yu-Xin
Format:	Artikel
Sprache:	eng
Schlagworte:	Autosomal Autosomal dominant nocturnal frontal epilepsy CHRNA7 dominant epilepsy frontal Gene Mutation nocturnal Polymorphism
Online-Zugang:	Volltext
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