Literature DB >> 28704742

Q10R mutation in SCN9A gene is associated with generalized epilepsy with febrile seizures plus.

Zhidong Cen1, Yuting Lou1, Yufan Guo1, Jianda Wang1, Jianhua Feng2.   

Abstract

Entities:  

Keywords:  Clinical heterogeneity; Generalized epilepsy with febrile seizures plus; Q10R mutation; SCN9A

Mesh：

Substances：

Year:  2017        PMID： 28704742     DOI： 10.1016/j.seizure.2017.06.023

Source DB:  PubMed          Journal:  Seizure        ISSN： 1059-1311            Impact factor:   3.184


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  4 in total

Review 1.  Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.

Authors:  Mark D Baker; Mohammed A Nassar
Journal:  Pflugers Arch       Date:  2020-06-29       Impact factor: 3.657

Review 2.  Channelopathy of Dravet Syndrome and Potential Neuroprotective Effects of Cannabidiol.

Authors:  Changqing Xu; Yumin Zhang; David Gozal; Paul Carney
Journal:  J Cent Nerv Syst Dis       Date:  2021-12-20

3.  Novel mutation of SCN9A gene causing generalized epilepsy with febrile seizures plus in a Chinese family.

Authors:  Tian Zhang; Mingwu Chen; Angang Zhu; Xiaoguang Zhang; Tao Fang
Journal:  Neurol Sci       Date:  2020-02-15       Impact factor: 3.307

4.  No association between SCN9A and monogenic human epilepsy disorders.

Authors:  James Fasham; Joseph S Leslie; Jamie W Harrison; James Deline; Katie B Williams; Ashley Kuhl; Jessica Scott Schwoerer; Harold E Cross; Andrew H Crosby; Emma L Baple
Journal:  PLoS Genet       Date:  2020-11-20       Impact factor: 6.020
  4 in total

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