GARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment.

Saved in:
Bibliographic Details
Title: GARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment.
Authors: Markovitz R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Ghosh R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Kuo ME; Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan.; Medical Scientist Training Program, University of Michigan, Ann Arbor, Michigan., Hong W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas., Lim J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas., Bernes S; Division of Child Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona., Manberg S; Division of Child Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona., Crosby K; Division of Genetics and Metabolism, Children's National Hospital, Rare Disease Institute, Washington, District of Columbia., Tanpaiboon P; Division of Genetics and Metabolism, Children's National Hospital, Rare Disease Institute, Washington, District of Columbia., Bharucha-Goebel D; Division of Neurology, Children's National Hospital, Washington, District of Columbia.; Neuromuscular and Neurogenetic Disorders of Childhood Section, NINDS, National Institutes of Health, Bethesda, Maryland., Bonnemann C; Division of Neurology, Children's National Hospital, Washington, District of Columbia.; Neuromuscular and Neurogenetic Disorders of Childhood Section, NINDS, National Institutes of Health, Bethesda, Maryland., Mohila CA; Department of Pathology, Texas Children's Hospital, Houston, Texas.; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas., Mizerik E; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas., Woodbury S; Texas Children's Hospital, Houston, Texas.; Baylor College of Medicine, Department of Physical Medicine and Rehabilitation, Houston, Texas., Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Lotze T; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas., Antonellis A; Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan.; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan.; Department of Neurology, University of Michigan, Ann Arbor, Michigan., Xiao R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Potocki L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2020 May; Vol. 182 (5), pp. 1167-1176. Date of Electronic Publication: 2020 Mar 17.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 32181591
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: GARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Markovitz+R%22">Markovitz R</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Ghosh+R%22">Ghosh R</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Kuo+ME%22">Kuo ME</searchLink>; Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan.; Medical Scientist Training Program, University of Michigan, Ann Arbor, Michigan.<br /><searchLink fieldCode="AU" term="%22Hong+W%22">Hong W</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Lim+J%22">Lim J</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Bernes+S%22">Bernes S</searchLink>; Division of Child Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona.<br /><searchLink fieldCode="AU" term="%22Manberg+S%22">Manberg S</searchLink>; Division of Child Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona.<br /><searchLink fieldCode="AU" term="%22Crosby+K%22">Crosby K</searchLink>; Division of Genetics and Metabolism, Children's National Hospital, Rare Disease Institute, Washington, District of Columbia.<br /><searchLink fieldCode="AU" term="%22Tanpaiboon+P%22">Tanpaiboon P</searchLink>; Division of Genetics and Metabolism, Children's National Hospital, Rare Disease Institute, Washington, District of Columbia.<br /><searchLink fieldCode="AU" term="%22Bharucha-Goebel+D%22">Bharucha-Goebel D</searchLink>; Division of Neurology, Children's National Hospital, Washington, District of Columbia.; Neuromuscular and Neurogenetic Disorders of Childhood Section, NINDS, National Institutes of Health, Bethesda, Maryland.<br /><searchLink fieldCode="AU" term="%22Bonnemann+C%22">Bonnemann C</searchLink>; Division of Neurology, Children's National Hospital, Washington, District of Columbia.; Neuromuscular and Neurogenetic Disorders of Childhood Section, NINDS, National Institutes of Health, Bethesda, Maryland.<br /><searchLink fieldCode="AU" term="%22Mohila+CA%22">Mohila CA</searchLink>; Department of Pathology, Texas Children's Hospital, Houston, Texas.; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Mizerik+E%22">Mizerik E</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Woodbury+S%22">Woodbury S</searchLink>; Texas Children's Hospital, Houston, Texas.; Baylor College of Medicine, Department of Physical Medicine and Rehabilitation, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Bi+W%22">Bi W</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Lotze+T%22">Lotze T</searchLink>; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Antonellis+A%22">Antonellis A</searchLink>; Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan.; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan.; Department of Neurology, University of Michigan, Ann Arbor, Michigan.<br /><searchLink fieldCode="AU" term="%22Xiao+R%22">Xiao R</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.<br /><searchLink fieldCode="AU" term="%22Potocki+L%22">Potocki L</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2020 May; Vol. 182 (5), pp. 1167-1176. <i>Date of Electronic Publication: </i>2020 Mar 17.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, N.I.H., Extramural
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32181591
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/ajmg.a.61544
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1167
    Titles:
      – TitleFull: GARS-related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Markovitz R
      – PersonEntity:
          Name:
            NameFull: Ghosh R
      – PersonEntity:
          Name:
            NameFull: Kuo ME
      – PersonEntity:
          Name:
            NameFull: Hong W
      – PersonEntity:
          Name:
            NameFull: Lim J
      – PersonEntity:
          Name:
            NameFull: Bernes S
      – PersonEntity:
          Name:
            NameFull: Manberg S
      – PersonEntity:
          Name:
            NameFull: Crosby K
      – PersonEntity:
          Name:
            NameFull: Tanpaiboon P
      – PersonEntity:
          Name:
            NameFull: Bharucha-Goebel D
      – PersonEntity:
          Name:
            NameFull: Bonnemann C
      – PersonEntity:
          Name:
            NameFull: Mohila CA
      – PersonEntity:
          Name:
            NameFull: Mizerik E
      – PersonEntity:
          Name:
            NameFull: Woodbury S
      – PersonEntity:
          Name:
            NameFull: Bi W
      – PersonEntity:
          Name:
            NameFull: Lotze T
      – PersonEntity:
          Name:
            NameFull: Antonellis A
      – PersonEntity:
          Name:
            NameFull: Xiao R
      – PersonEntity:
          Name:
            NameFull: Potocki L
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 05
              Text: 2020 May
              Type: published
              Y: 2020
          Identifiers:
            – Type: issn-electronic
              Value: 1552-4833
          Numbering:
            – Type: volume
              Value: 182
            – Type: issue
              Value: 5
          Titles:
            – TitleFull: American journal of medical genetics. Part A
              Type: main
ResultId 1