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Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.

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Title: Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.
Authors: Cui F; Department of Molecular Genetics, Chifeng Maternity Hospital, Chifeng, China., Wulan T; Department of Reproduction, Chifeng Maternity Hospital, Chifeng, China., Zhang Q; AmCare Genomics Lab, Guangzhou, China., Zhang VW; AmCare Genomics Lab, Guangzhou, China., Jiang Y; Department of Obstetrics, Chifeng Maternity Hospital, Chifeng, China.
Source: Frontiers in genetics [Front Genet] 2024 Mar 06; Vol. 15, pp. 1371282. Date of Electronic Publication: 2024 Mar 06 (Print Publication: 2024).
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.
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  Data: <searchLink fieldCode="AU" term="%22Cui+F%22">Cui F</searchLink>; Department of Molecular Genetics, Chifeng Maternity Hospital, Chifeng, China.<br /><searchLink fieldCode="AU" term="%22Wulan+T%22">Wulan T</searchLink>; Department of Reproduction, Chifeng Maternity Hospital, Chifeng, China.<br /><searchLink fieldCode="AU" term="%22Zhang+Q%22">Zhang Q</searchLink>; AmCare Genomics Lab, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Zhang+VW%22">Zhang VW</searchLink>; AmCare Genomics Lab, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Jiang+Y%22">Jiang Y</searchLink>; Department of Obstetrics, Chifeng Maternity Hospital, Chifeng, China.
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  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2024 Mar 06; Vol. 15, pp. 1371282. <i>Date of Electronic Publication: </i>2024 Mar 06 (<i>Print Publication: </i>2024).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.3389/fgene.2024.1371282
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        Text: English
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      – TitleFull: Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.
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            – D: 06
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              Text: 2024 Mar 06
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