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Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: a single-center cohort study.

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Title: Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: a single-center cohort study.
Authors: Hu, Junji1 (AUTHOR), Xin, Min2 (AUTHOR), Liu, Jinxiu2 (AUTHOR), Li, Hongxing1 (AUTHOR), Li, Xuemei1 (AUTHOR), Chen, Longchang1 (AUTHOR), Yang, Ping1 (AUTHOR), Zhao, Haiyan1 (AUTHOR), Sun, Pengfei1 (AUTHOR), Gao, Guodong1 (AUTHOR), Feng, Hu1 (AUTHOR), Li, Zhongxia1 (AUTHOR), Xiao, Guang1 (AUTHOR), Li, Yu1 (AUTHOR), Li, Kun1,3 (AUTHOR) 593190230@qq.com, Xu, Xinsheng1,3 (AUTHOR) zgdxbw@163.com
Source: BMC Medical Genomics. 7/15/2025, Vol. 18 Issue 1, p1-16. 16p.
Database: Academic Search Ultimate
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  Data: Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: a single-center cohort study.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 7/15/2025, Vol. 18 Issue 1, p1-16. 16p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186644799
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        Value: 10.1186/s12920-025-02184-7
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        Text: English
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              Text: 7/15/2025
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