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A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.

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Title: A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.
Authors: Penkl, Anja1, Reunert, Janine1, Debus, Otfried M.2, Homann, Anna3, Och, Ulrike1, Rust, Stephan1, Marquardt, Thorsten1, marquat@uni-muenster.de
Source: American Journal of Medical Genetics. Part A; Mar2022, Vol. 188 Issue 3, p941-947, 7p
Database: Applied Science & Technology Source
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  Availability: 0
Header DbId: aci
DbLabel: Applied Science & Technology Source
An: 155218007
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.
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  Data: <searchLink fieldCode="AU" term="%22Penkl%2C+Anja%22">Penkl, Anja</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Reunert%2C+Janine%22">Reunert, Janine</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Debus%2C+Otfried+M%2E%22">Debus, Otfried M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AU" term="%22Homann%2C+Anna%22">Homann, Anna</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AU" term="%22Och%2C+Ulrike%22">Och, Ulrike</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Rust%2C+Stephan%22">Rust, Stephan</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Marquardt%2C+Thorsten%22">Marquardt, Thorsten</searchLink><relatesTo>1</relatesTo>, <i>marquat@uni-muenster.de</i>
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  Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; Mar2022, Vol. 188 Issue 3, p941-947, 7p
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=155218007
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/ajmg.a.62581
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      – Code: eng
        Text: English
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        PageCount: 7
        StartPage: 941
    Titles:
      – TitleFull: A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.
        Type: main
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      – PersonEntity:
          Name:
            NameFull: Penkl, Anja
      – PersonEntity:
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            NameFull: Reunert, Janine
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            NameFull: Debus, Otfried M.
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            NameFull: Homann, Anna
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            NameFull: Och, Ulrike
      – PersonEntity:
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            NameFull: Rust, Stephan
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            NameFull: Marquardt, Thorsten
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          Dates:
            – D: 01
              M: 03
              Text: Mar2022
              Type: published
              Y: 2022
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              Value: 188
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              Value: 3
          Titles:
            – TitleFull: American Journal of Medical Genetics. Part A
              Type: main
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