View in EDS HTML Full Text PDF Full Text

ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38.

Saved in:
Bibliographic Details
Title: ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38.
Authors: Neissi, Mostafa1,2,3 (AUTHOR) iammostafaneissi@gmail.com, Al-Zaalan, Ayoob Radhi4 (AUTHOR), Mohammadi-Asl, Misagh3 (AUTHOR), Roghani, Mojdeh3 (AUTHOR), Mohammadi-Asl, Javad3,5 (AUTHOR), Jorfi, Kamele3 (AUTHOR) kamelejorfi@gmail.com
Source: Journal of Rare Diseases. 2/5/2025, Vol. 4 Issue 1, p1-8. 8p.
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: 182843171
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Neissi%2C+Mostafa%22">Neissi, Mostafa</searchLink><relatesTo>1,2,3</relatesTo> (AUTHOR)<i> iammostafaneissi@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Al-Zaalan%2C+Ayoob+Radhi%22">Al-Zaalan, Ayoob Radhi</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mohammadi-Asl%2C+Misagh%22">Mohammadi-Asl, Misagh</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Roghani%2C+Mojdeh%22">Roghani, Mojdeh</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mohammadi-Asl%2C+Javad%22">Mohammadi-Asl, Javad</searchLink><relatesTo>3,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jorfi%2C+Kamele%22">Jorfi, Kamele</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> kamelejorfi@gmail.com</i>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Journal+of+Rare+Diseases%22">Journal of Rare Diseases</searchLink>. 2/5/2025, Vol. 4 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=182843171
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1007/s44162-025-00066-1
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 8
        StartPage: 1
    Titles:
      – TitleFull: ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Neissi, Mostafa
      – PersonEntity:
          Name:
            NameFull: Al-Zaalan, Ayoob Radhi
      – PersonEntity:
          Name:
            NameFull: Mohammadi-Asl, Misagh
      – PersonEntity:
          Name:
            NameFull: Roghani, Mojdeh
      – PersonEntity:
          Name:
            NameFull: Mohammadi-Asl, Javad
      – PersonEntity:
          Name:
            NameFull: Jorfi, Kamele
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 05
              M: 02
              Text: 2/5/2025
              Type: published
              Y: 2025
          Identifiers:
            – Type: issn-print
              Value: 2731085X
          Numbering:
            – Type: volume
              Value: 4
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Journal of Rare Diseases
              Type: main
ResultId 1