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Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.

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Title: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.
Authors: Helman G, Takanohashi A, Hagemann TL, Perng MD, Walkiewicz M, Woidill S, Sase S, Cross Z, Du Y, Zhao L, Waldman A, Haake BC, Fatemi A, Brenner M, Sherbini O, Messing A, Vanderver A, Simons C
Source: Human mutation [Hum Mutat] 2022 Sep; Vol. 43 (9), pp. 1344.
Publication Type: Published Erratum
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 35920398
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  Data: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.
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  Data: <searchLink fieldCode="AU" term="%22Helman+G%22">Helman G</searchLink><br /><searchLink fieldCode="AU" term="%22Takanohashi+A%22">Takanohashi A</searchLink><br /><searchLink fieldCode="AU" term="%22Hagemann+TL%22">Hagemann TL</searchLink><br /><searchLink fieldCode="AU" term="%22Perng+MD%22">Perng MD</searchLink><br /><searchLink fieldCode="AU" term="%22Walkiewicz+M%22">Walkiewicz M</searchLink><br /><searchLink fieldCode="AU" term="%22Woidill+S%22">Woidill S</searchLink><br /><searchLink fieldCode="AU" term="%22Sase+S%22">Sase S</searchLink><br /><searchLink fieldCode="AU" term="%22Cross+Z%22">Cross Z</searchLink><br /><searchLink fieldCode="AU" term="%22Du+Y%22">Du Y</searchLink><br /><searchLink fieldCode="AU" term="%22Zhao+L%22">Zhao L</searchLink><br /><searchLink fieldCode="AU" term="%22Waldman+A%22">Waldman A</searchLink><br /><searchLink fieldCode="AU" term="%22Haake+BC%22">Haake BC</searchLink><br /><searchLink fieldCode="AU" term="%22Fatemi+A%22">Fatemi A</searchLink><br /><searchLink fieldCode="AU" term="%22Brenner+M%22">Brenner M</searchLink><br /><searchLink fieldCode="AU" term="%22Sherbini+O%22">Sherbini O</searchLink><br /><searchLink fieldCode="AU" term="%22Messing+A%22">Messing A</searchLink><br /><searchLink fieldCode="AU" term="%22Vanderver+A%22">Vanderver A</searchLink><br /><searchLink fieldCode="AU" term="%22Simons+C%22">Simons C</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2022 Sep; Vol. 43 (9), pp. 1344.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>PubMed not MEDLINE
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      – Type: doi
        Value: 10.1002/humu.24400
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1344
    Titles:
      – TitleFull: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.
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            NameFull: Helman G
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            – D: 01
              M: 09
              Text: 2022 Sep
              Type: published
              Y: 2022
          Identifiers:
            – Type: issn-electronic
              Value: 1098-1004
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            – Type: volume
              Value: 43
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: Human mutation
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