View in EDS

Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.

Saved in:
Bibliographic Details
Title: Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.
Authors: Fuchs SA; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl., Schene IF; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Kok G; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Jansen JM; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Nikkels PGJ; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands., van Gassen KLI; Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands., Terheggen-Lagro SWJ; Department of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands., van der Crabben SN; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Hoeks SE; Department of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands., Niers LEM; Department of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands., Wolf NI; Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands., de Vries MC; Nijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands., Koolen DA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Houwen RHJ; Division of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands., Mulder MF; Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands., van Hasselt PM; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Oct; Vol. 23 (10), pp. 2024.
Publication Type: Published Erratum
Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE; PubMed not MEDLINE
Database: MEDLINE Ultimate
FullText Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 32934367
AccessLevel: 2
PubTypeId: unknown
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Fuchs+SA%22">Fuchs SA</searchLink>; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl.<br /><searchLink fieldCode="AU" term="%22Schene+IF%22">Schene IF</searchLink>; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kok+G%22">Kok G</searchLink>; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Jansen+JM%22">Jansen JM</searchLink>; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Nikkels+PGJ%22">Nikkels PGJ</searchLink>; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Gassen+KLI%22">van Gassen KLI</searchLink>; Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Terheggen-Lagro+SWJ%22">Terheggen-Lagro SWJ</searchLink>; Department of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+der+Crabben+SN%22">van der Crabben SN</searchLink>; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Hoeks+SE%22">Hoeks SE</searchLink>; Department of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Niers+LEM%22">Niers LEM</searchLink>; Department of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Wolf+NI%22">Wolf NI</searchLink>; Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22de+Vries+MC%22">de Vries MC</searchLink>; Nijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Koolen+DA%22">Koolen DA</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Houwen+RHJ%22">Houwen RHJ</searchLink>; Division of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Mulder+MF%22">Mulder MF</searchLink>; Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Hasselt+PM%22">van Hasselt PM</searchLink>; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229815831%22">Genetics in medicine : official journal of the American College of Medical Genetics</searchLink> [Genet Med] 2021 Oct; Vol. 23 (10), pp. 2024.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Published Erratum
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9815831 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1530-0366 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210983600%22">10983600 </searchLink><i>NLM ISO Abbreviation: </i>Genet Med <i>Subsets: </i>MEDLINE; PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32934367
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1038/s41436-020-00966-1
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 2024
    Titles:
      – TitleFull: Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Fuchs SA
      – PersonEntity:
          Name:
            NameFull: Schene IF
      – PersonEntity:
          Name:
            NameFull: Kok G
      – PersonEntity:
          Name:
            NameFull: Jansen JM
      – PersonEntity:
          Name:
            NameFull: Nikkels PGJ
      – PersonEntity:
          Name:
            NameFull: van Gassen KLI
      – PersonEntity:
          Name:
            NameFull: Terheggen-Lagro SWJ
      – PersonEntity:
          Name:
            NameFull: van der Crabben SN
      – PersonEntity:
          Name:
            NameFull: Hoeks SE
      – PersonEntity:
          Name:
            NameFull: Niers LEM
      – PersonEntity:
          Name:
            NameFull: Wolf NI
      – PersonEntity:
          Name:
            NameFull: de Vries MC
      – PersonEntity:
          Name:
            NameFull: Koolen DA
      – PersonEntity:
          Name:
            NameFull: Houwen RHJ
      – PersonEntity:
          Name:
            NameFull: Mulder MF
      – PersonEntity:
          Name:
            NameFull: van Hasselt PM
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 10
              Text: 2021 Oct
              Type: published
              Y: 2021
          Identifiers:
            – Type: issn-electronic
              Value: 1530-0366
          Numbering:
            – Type: volume
              Value: 23
            – Type: issue
              Value: 10
          Titles:
            – TitleFull: Genetics in medicine : official journal of the American College of Medical Genetics
              Type: main
ResultId 1