View in EDS HTML Full Text PDF Full Text

Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review.

Saved in:
Bibliographic Details
Title: Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review.
Authors: Cherkaoui, Imane1 (AUTHOR), Lhousni, Saida1,2 (AUTHOR), Elouali, Aziza3 (AUTHOR), Elidrissi Errahhali, Mounia1,2 (AUTHOR), Elidrissi Errahhali, Manal1,2 (AUTHOR), Charif, Majida4 (AUTHOR), Ouarzane, Meryem1,2 (AUTHOR), Rkain, Maria3 (AUTHOR), Sellam, Adnane5,6 (AUTHOR), Boulouiz, Redouane1,2 (AUTHOR), Bellaoui, Mohammed1,2 (AUTHOR) bmbellaoui@gmail.com
Source: Journal of Rare Diseases. 7/7/2026, Vol. 5 Issue 1, p1-6. 6p.
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: 195150700
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Cherkaoui%2C+Imane%22">Cherkaoui, Imane</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lhousni%2C+Saida%22">Lhousni, Saida</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Elouali%2C+Aziza%22">Elouali, Aziza</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Elidrissi+Errahhali%2C+Mounia%22">Elidrissi Errahhali, Mounia</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Elidrissi+Errahhali%2C+Manal%22">Elidrissi Errahhali, Manal</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Charif%2C+Majida%22">Charif, Majida</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ouarzane%2C+Meryem%22">Ouarzane, Meryem</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rkain%2C+Maria%22">Rkain, Maria</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sellam%2C+Adnane%22">Sellam, Adnane</searchLink><relatesTo>5,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Boulouiz%2C+Redouane%22">Boulouiz, Redouane</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bellaoui%2C+Mohammed%22">Bellaoui, Mohammed</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> bmbellaoui@gmail.com</i>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Journal+of+Rare+Diseases%22">Journal of Rare Diseases</searchLink>. 7/7/2026, Vol. 5 Issue 1, p1-6. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=195150700
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1007/s44162-026-00216-z
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 6
        StartPage: 1
    Titles:
      – TitleFull: Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Cherkaoui, Imane
      – PersonEntity:
          Name:
            NameFull: Lhousni, Saida
      – PersonEntity:
          Name:
            NameFull: Elouali, Aziza
      – PersonEntity:
          Name:
            NameFull: Elidrissi Errahhali, Mounia
      – PersonEntity:
          Name:
            NameFull: Elidrissi Errahhali, Manal
      – PersonEntity:
          Name:
            NameFull: Charif, Majida
      – PersonEntity:
          Name:
            NameFull: Ouarzane, Meryem
      – PersonEntity:
          Name:
            NameFull: Rkain, Maria
      – PersonEntity:
          Name:
            NameFull: Sellam, Adnane
      – PersonEntity:
          Name:
            NameFull: Boulouiz, Redouane
      – PersonEntity:
          Name:
            NameFull: Bellaoui, Mohammed
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 07
              M: 07
              Text: 7/7/2026
              Type: published
              Y: 2026
          Identifiers:
            – Type: issn-print
              Value: 2731085X
          Numbering:
            – Type: volume
              Value: 5
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Journal of Rare Diseases
              Type: main
ResultId 1