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SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.

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Title: SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.
Authors: Arlt, Annabelle1,2 (AUTHOR), Akova-Öztürk, Esra2 (AUTHOR), Schirmacher, Anja3 (AUTHOR), Schlüter, Bernhard3 (AUTHOR), Rust, Stephan3,4 (AUTHOR), Meyer zu Hörste, Gerd2 (AUTHOR), Wiendl, Heinz2 (AUTHOR), Wiethoff, Sarah2,5 (AUTHOR) sarah.wiethoff@ukmuenster.de
Source: Journal of Neurogenetics. Jun2024, Vol. 38 Issue 2, p35-40. 6p.
Database: Academic Search Ultimate
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An: 178587452
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  Data: SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.
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  Data: <searchLink fieldCode="AR" term="%22Arlt%2C+Annabelle%22">Arlt, Annabelle</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Akova-Öztürk%2C+Esra%22">Akova-Öztürk, Esra</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schirmacher%2C+Anja%22">Schirmacher, Anja</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schlüter%2C+Bernhard%22">Schlüter, Bernhard</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rust%2C+Stephan%22">Rust, Stephan</searchLink><relatesTo>3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Meyer+zu+Hörste%2C+Gerd%22">Meyer zu Hörste, Gerd</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wiendl%2C+Heinz%22">Wiendl, Heinz</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wiethoff%2C+Sarah%22">Wiethoff, Sarah</searchLink><relatesTo>2,5</relatesTo> (AUTHOR)<i> sarah.wiethoff@ukmuenster.de</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Neurogenetics%22">Journal of Neurogenetics</searchLink>. Jun2024, Vol. 38 Issue 2, p35-40. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=178587452
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1080/01677063.2024.2374898
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 6
        StartPage: 35
    Titles:
      – TitleFull: SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.
        Type: main
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          Name:
            NameFull: Arlt, Annabelle
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            NameFull: Akova-Öztürk, Esra
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            NameFull: Schirmacher, Anja
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            NameFull: Schlüter, Bernhard
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            NameFull: Rust, Stephan
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            NameFull: Meyer zu Hörste, Gerd
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            NameFull: Wiendl, Heinz
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            NameFull: Wiethoff, Sarah
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          Dates:
            – D: 01
              M: 06
              Text: Jun2024
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 01677063
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              Value: 38
            – Type: issue
              Value: 2
          Titles:
            – TitleFull: Journal of Neurogenetics
              Type: main
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