A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis.
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| Title: | A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis. |
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| Authors: | Kitzmüller C; MRC Laboratory for Molecular Cell Biology, UCL Institute of Child Health, University College London, UK., Haines RL, Codlin S, Cutler DF, Mole SE |
| Source: | Human molecular genetics [Hum Mol Genet] 2008 Jan 15; Vol. 17 (2), pp. 303-12. Date of Electronic Publication: 2007 Oct 18. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 17947292 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kitzmüller+C%22">Kitzmüller C</searchLink>; MRC Laboratory for Molecular Cell Biology, UCL Institute of Child Health, University College London, UK.<br /><searchLink fieldCode="AU" term="%22Haines+RL%22">Haines RL</searchLink><br /><searchLink fieldCode="AU" term="%22Codlin+S%22">Codlin S</searchLink><br /><searchLink fieldCode="AU" term="%22Cutler+DF%22">Cutler DF</searchLink><br /><searchLink fieldCode="AU" term="%22Mole+SE%22">Mole SE</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2008 Jan 15; Vol. 17 (2), pp. 303-12. <i>Date of Electronic Publication: </i>2007 Oct 18. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=17947292 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddm306 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 303 Titles: – TitleFull: A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kitzmüller C – PersonEntity: Name: NameFull: Haines RL – PersonEntity: Name: NameFull: Codlin S – PersonEntity: Name: NameFull: Cutler DF – PersonEntity: Name: NameFull: Mole SE IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 01 Text: 2008 Jan 15 Type: published Y: 2008 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 17 – Type: issue Value: 2 Titles: – TitleFull: Human molecular genetics Type: main |
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