Records 1 - 8 (of 8 Records)
|Query Trace: Epilepsy and CHRNB2[original query]|
| A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely.
Neuroscience letters 2007 Jul 422 (1): 74-6.
Gu Wenli, Bertrand Daniel, Steinlein Ortrud
| Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits.
Journal of clinical laboratory analysis 2007 21 (2): 67-70.
Lee Cheng-Chun, Chou I-Ching, Tsai Chang-Hai, Wan Lei, Shu Yu-An, Tsai Yuhsin, Li Tsai-Chung, Tsai Fuu-J
| A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy.
Epilepsy research 2009 Feb 83 (2-3): 152-6.
Chen Yan, Wu Liwen, Fang Yue, He Zhiyi, Peng Bingwei, Shen Yan, Xu
| CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients.
Sleep medicine 2009 Jan 10 (1): 139-42.
Combi Romina, Ferini-Strambi Luigi, Tenchini Maria Lui
| The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy.
Epilepsy research 2011 Jun 95 (1-2): 94-9.
Liu Hui, Lu Cailing, Li Zhenzhong, Zhou Shiyi, Li Xiaoqiao, Ji Liri, Lu Qiang, Lv Ruijuan, Wu Liwen, Ma
| [Mutational analysis of CHRNB2 and CHRNA2 genes in southern Chinese population with autosomal dominant nocturnal frontal lobe epilepsy].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2011 Feb 28 (1): 14-8.
Chen Zhi-hong, Zhai Qiong-xiang, Gui Juan, Zhang Yu-xin, Guo Yu-xiong, Ding Jian, Hao Yi
| Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy.
International journal of clinical and experimental medicine 2015 8 (6): 9063-70.
Chen Zhihong, Wang Lingan, Wang Chun, Chen Qian, Zhai Qiongxiang, Guo Yuxiong, Zhang Yux
| Familial Epilepsy Associated With Concurrent CHRNB2 Mutation and RBFOX1 Exon Deletion: A Case Report.
Cureus 2023 4 15 (3): e35845.
Xu Tony, Luong Dorris, Zhong Ni
- Page last reviewed:Oct 1, 2023
- Page last updated:Nov 30, 2023
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