Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature.
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| Title: | Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. |
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| Authors: | Vuillaume ML, Moizard MP, Rossignol S, Cottereau E, Vonwill S, Alessandri JL, Busa T, Colin E, Gérard M, Giuliano F, Lambert L, Lefevre M, Kotecha U, Nampoothiri S, Netchine I, Raynaud M, Brioude F, Toutain A |
| Source: | Human mutation [Hum Mutat] 2018 Dec; Vol. 39 (12), pp. 2110-2112. Date of Electronic Publication: 2018 Sep 17. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 30447178 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Vuillaume+ML%22">Vuillaume ML</searchLink><br /><searchLink fieldCode="AU" term="%22Moizard+MP%22">Moizard MP</searchLink><br /><searchLink fieldCode="AU" term="%22Rossignol+S%22">Rossignol S</searchLink><br /><searchLink fieldCode="AU" term="%22Cottereau+E%22">Cottereau E</searchLink><br /><searchLink fieldCode="AU" term="%22Vonwill+S%22">Vonwill S</searchLink><br /><searchLink fieldCode="AU" term="%22Alessandri+JL%22">Alessandri JL</searchLink><br /><searchLink fieldCode="AU" term="%22Busa+T%22">Busa T</searchLink><br /><searchLink fieldCode="AU" term="%22Colin+E%22">Colin E</searchLink><br /><searchLink fieldCode="AU" term="%22Gérard+M%22">Gérard M</searchLink><br /><searchLink fieldCode="AU" term="%22Giuliano+F%22">Giuliano F</searchLink><br /><searchLink fieldCode="AU" term="%22Lambert+L%22">Lambert L</searchLink><br /><searchLink fieldCode="AU" term="%22Lefevre+M%22">Lefevre M</searchLink><br /><searchLink fieldCode="AU" term="%22Kotecha+U%22">Kotecha U</searchLink><br /><searchLink fieldCode="AU" term="%22Nampoothiri+S%22">Nampoothiri S</searchLink><br /><searchLink fieldCode="AU" term="%22Netchine+I%22">Netchine I</searchLink><br /><searchLink fieldCode="AU" term="%22Raynaud+M%22">Raynaud M</searchLink><br /><searchLink fieldCode="AU" term="%22Brioude+F%22">Brioude F</searchLink><br /><searchLink fieldCode="AU" term="%22Toutain+A%22">Toutain A</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2018 Dec; Vol. 39 (12), pp. 2110-2112. <i>Date of Electronic Publication: </i>2018 Sep 17. – 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="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print-Electronic <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>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=30447178 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/humu.23612 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2110 Titles: – TitleFull: Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Vuillaume ML – PersonEntity: Name: NameFull: Moizard MP – PersonEntity: Name: NameFull: Rossignol S – PersonEntity: Name: NameFull: Cottereau E – PersonEntity: Name: NameFull: Vonwill S – PersonEntity: Name: NameFull: Alessandri JL – PersonEntity: Name: NameFull: Busa T – PersonEntity: Name: NameFull: Colin E – PersonEntity: Name: NameFull: Gérard M – PersonEntity: Name: NameFull: Giuliano F – PersonEntity: Name: NameFull: Lambert L – PersonEntity: Name: NameFull: Lefevre M – PersonEntity: Name: NameFull: Kotecha U – PersonEntity: Name: NameFull: Nampoothiri S – PersonEntity: Name: NameFull: Netchine I – PersonEntity: Name: NameFull: Raynaud M – PersonEntity: Name: NameFull: Brioude F – PersonEntity: Name: NameFull: Toutain A IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2018 Dec Type: published Y: 2018 Identifiers: – Type: issn-electronic Value: 1098-1004 Numbering: – Type: volume Value: 39 – Type: issue Value: 12 Titles: – TitleFull: Human mutation Type: main |
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