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Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis.

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Title: Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis.
Authors: Sharp JD; Department of Paediatrics and Child Health, Royal Free and University College Medical School, University College London, London, UK., Wheeler RB, Parker KA, Gardiner RM, Williams RE, Mole SE
Source: Human mutation [Hum Mutat] 2003 Jul; Vol. 22 (1), pp. 35-42.
Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis.
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  Data: <searchLink fieldCode="AU" term="%22Sharp+JD%22">Sharp JD</searchLink>; Department of Paediatrics and Child Health, Royal Free and University College Medical School, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Wheeler+RB%22">Wheeler RB</searchLink><br /><searchLink fieldCode="AU" term="%22Parker+KA%22">Parker KA</searchLink><br /><searchLink fieldCode="AU" term="%22Gardiner+RM%22">Gardiner RM</searchLink><br /><searchLink fieldCode="AU" term="%22Williams+RE%22">Williams RE</searchLink><br /><searchLink fieldCode="AU" term="%22Mole+SE%22">Mole SE</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2003 Jul; Vol. 22 (1), pp. 35-42.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=12815591
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1002/humu.10227
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 35
    Titles:
      – TitleFull: Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis.
        Type: main
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      – PersonEntity:
          Name:
            NameFull: Sharp JD
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          Name:
            NameFull: Wheeler RB
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            NameFull: Parker KA
      – PersonEntity:
          Name:
            NameFull: Gardiner RM
      – PersonEntity:
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            NameFull: Williams RE
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            NameFull: Mole SE
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          Dates:
            – D: 01
              M: 07
              Text: 2003 Jul
              Type: published
              Y: 2003
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              Value: 1098-1004
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              Value: 22
            – Type: issue
              Value: 1
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            – TitleFull: Human mutation
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