Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.

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Title: Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.
Authors: Gong P; Department of Pediatrics, Peking University First Hospital, Beijing, China., Jiao X; Department of Pediatrics, Peking University First Hospital, Beijing, China., Yu D; Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China., Yang Z; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Source: Frontiers in genetics [Front Genet] 2021 Jun 30; Vol. 12, pp. 649556. Date of Electronic Publication: 2021 Jun 30 (Print Publication: 2021).
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: Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.
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  Data: <searchLink fieldCode="AU" term="%22Gong+P%22">Gong P</searchLink>; Department of Pediatrics, Peking University First Hospital, Beijing, China.<br /><searchLink fieldCode="AU" term="%22Jiao+X%22">Jiao X</searchLink>; Department of Pediatrics, Peking University First Hospital, Beijing, China.<br /><searchLink fieldCode="AU" term="%22Yu+D%22">Yu D</searchLink>; Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.<br /><searchLink fieldCode="AU" term="%22Yang+Z%22">Yang Z</searchLink>; Department of Pediatrics, Peking University First Hospital, Beijing, China.
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  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2021 Jun 30; Vol. 12, pp. 649556. <i>Date of Electronic Publication: </i>2021 Jun 30 (<i>Print Publication: </i>2021).
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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.2021.649556
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        Text: English
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      – TitleFull: Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.
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            NameFull: Gong P
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            NameFull: Jiao X
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            NameFull: Yu D
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              Text: 2021 Jun 30
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              Y: 2021
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