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Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.

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Title: Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.
Authors: Issa FA; Department of Physiology, University of California at Los Angeles, Los Angeles, CA 90095-1751, USA., Mock AF, Sagasti A, Papazian DM
Source: Disease models & mechanisms [Dis Model Mech] 2012 Nov; Vol. 5 (6), pp. 921-9. Date of Electronic Publication: 2012 Jun 26.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Company of Biologists Ltd Country of Publication: England NLM ID: 101483332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1754-8411 (Electronic) Linking ISSN: 17548403 NLM ISO Abbreviation: Dis Model Mech Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Availability: 0
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DbLabel: MEDLINE Ultimate
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AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.
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  Data: <searchLink fieldCode="AU" term="%22Issa+FA%22">Issa FA</searchLink>; Department of Physiology, University of California at Los Angeles, Los Angeles, CA 90095-1751, USA.<br /><searchLink fieldCode="AU" term="%22Mock+AF%22">Mock AF</searchLink><br /><searchLink fieldCode="AU" term="%22Sagasti+A%22">Sagasti A</searchLink><br /><searchLink fieldCode="AU" term="%22Papazian+DM%22">Papazian DM</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101483332%22">Disease models & mechanisms</searchLink> [Dis Model Mech] 2012 Nov; Vol. 5 (6), pp. 921-9. <i>Date of Electronic Publication: </i>2012 Jun 26.
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  Data: Journal Article; Research Support, N.I.H., Extramural
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Company+of+Biologists+Ltd%22">Company of Biologists Ltd </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101483332 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1754-8411 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217548403%22">17548403 </searchLink><i>NLM ISO Abbreviation: </i>Dis Model Mech <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=22736459
RecordInfo BibRecord:
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    Identifiers:
      – Type: doi
        Value: 10.1242/dmm.010157
    Languages:
      – Code: eng
        Text: English
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      Pagination:
        StartPage: 921
    Titles:
      – TitleFull: Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.
        Type: main
  BibRelationships:
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      – PersonEntity:
          Name:
            NameFull: Issa FA
      – PersonEntity:
          Name:
            NameFull: Mock AF
      – PersonEntity:
          Name:
            NameFull: Sagasti A
      – PersonEntity:
          Name:
            NameFull: Papazian DM
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 11
              Text: 2012 Nov
              Type: published
              Y: 2012
          Identifiers:
            – Type: issn-electronic
              Value: 1754-8411
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            – Type: volume
              Value: 5
            – Type: issue
              Value: 6
          Titles:
            – TitleFull: Disease models & mechanisms
              Type: main
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