Literature DB >> 28472029

Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.

Yimin Wang, Xiaonan Du, Rao Bin, Shanshan Yu, Zhezhi Xia, Guo Zheng, Jianmin Zhong, Yunjian Zhang, Yong-Hui Jiang, Yi Wang.   

Abstract

Entities:  

Year:  2017        PMID: 28472029      PMCID: PMC5417344          DOI: 10.1038/srep46520

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


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This Article contains a typographical error in the Results section under subheading “Targeted exome sequencing”, where: “Through this filtering process, we identified 24 SNVs [2 families (S86 and D1422) have compound heterozygotes and 2 families (D1339 and D1433) have more than 1 SNV] from 16 patients that are pathogenic or likely pathogenic (Table 1)”. should read: “Through this filtering process, we identified 24 SNVs [2 families (S86 and D1422) have compound heterozygotes and 2 families (D1339 and D1433) have more than 1 SNV] from 15 patients that are pathogenic or likely pathogenic (Table 1)”. In addition, the Supplementary Information File originally published with this Article contained errors in Supplementary Table S1. These errors have now been corrected in the Supplementary Information that accompanies the Article.
  2 in total

Review 1.  Voltage Gated Sodium Channel Genes in Epilepsy: Mutations, Functional Studies, and Treatment Dimensions.

Authors:  Ibitayo Abigail Ademuwagun; Solomon Oladapo Rotimi; Steffen Syrbe; Yvonne Ukamaka Ajamma; Ezekiel Adebiyi
Journal:  Front Neurol       Date:  2021-03-24       Impact factor: 4.003

2.  Clinical Study of 8 Cases of CHD2 Gene Mutation-Related Neurological Diseases and Their Mechanisms.

Authors:  Xiaona Luo; Xiaoang Sun; Yilin Wang; Longlong Lin; Fang Yuan; Simei Wang; Wenjing Zhang; Xiaobing Ji; Meiyan Liu; Shengnan Wu; Xiaoping Lan; Jie Zhang; Jingbin Yan; Fanyi Zeng; Yucai Chen
Journal:  Front Cell Dev Biol       Date:  2022-03-21
  2 in total

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