View in EDS HTML Full Text PDF Full Text

The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.

Saved in:
Bibliographic Details
Title: The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.
Authors: Mercan, Metin1 (AUTHOR) dr_metin_mercan@hotmail.com, Seyhan, Serhat2 (AUTHOR), Yayla, Vildan1 (AUTHOR)
Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug2025, Vol. 26 Issue 5/6, p573-590. 18p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 186807313
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Mercan%2C+Metin%22">Mercan, Metin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> dr_metin_mercan@hotmail.com</i><br /><searchLink fieldCode="AR" term="%22Seyhan%2C+Serhat%22">Seyhan, Serhat</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yayla%2C+Vildan%22">Yayla, Vildan</searchLink><relatesTo>1</relatesTo> (AUTHOR)
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Amyotrophic+Lateral+Sclerosis+%26+Frontotemporal+Degeneration%22">Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration</searchLink>. Aug2025, Vol. 26 Issue 5/6, p573-590. 18p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186807313
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1080/21678421.2025.2477732
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 18
        StartPage: 573
    Titles:
      – TitleFull: The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Mercan, Metin
      – PersonEntity:
          Name:
            NameFull: Seyhan, Serhat
      – PersonEntity:
          Name:
            NameFull: Yayla, Vildan
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 08
              Text: Aug2025
              Type: published
              Y: 2025
          Identifiers:
            – Type: issn-print
              Value: 21678421
          Numbering:
            – Type: volume
              Value: 26
            – Type: issue
              Value: 5/6
          Titles:
            – TitleFull: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
              Type: main
ResultId 1