Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/136/10/e254/11137526/awt141.pdf
Reference9 articles.
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2. Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus;Crompton;Arch Neurol,2012
3. Myoclonic disorders: a practical approach for diagnosis and treatment;Kojovic;Ther Adv Neurol Disord,2011
4. Drug-induced tremors;Morgan;Lancet Neurol,2005
5. Hippocampal sclerosis: progress since Sommer;Thom;Brain Pathol,2009
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Gene–gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsy;Neurogenetics;2024-03-09
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