Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.
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| Title: | Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. |
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| Authors: | Elsayed, Solaf M1, Heller, Raoul2, Thoenes, Michaela2, Zaki, Maha S3, Swan, Daniel4, Elsobky, Ezzat1, Zühlke, Christine5, Ebermann, Inga2, Nürnberg, Gudrun6, Nürnberg, Peter6, Bolz, Hanno J7 |
| Source: | European Journal of Human Genetics. Feb2014, Vol. 22 Issue 2, p286-288. 3p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 93707379 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Elsayed%2C+Solaf+M%22">Elsayed, Solaf M</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Heller%2C+Raoul%22">Heller, Raoul</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Thoenes%2C+Michaela%22">Thoenes, Michaela</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Zaki%2C+Maha+S%22">Zaki, Maha S</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Swan%2C+Daniel%22">Swan, Daniel</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Elsobky%2C+Ezzat%22">Elsobky, Ezzat</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Zühlke%2C+Christine%22">Zühlke, Christine</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Ebermann%2C+Inga%22">Ebermann, Inga</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Nürnberg%2C+Gudrun%22">Nürnberg, Gudrun</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Nürnberg%2C+Peter%22">Nürnberg, Peter</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Bolz%2C+Hanno+J%22">Bolz, Hanno J</searchLink><relatesTo>7</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Human+Genetics%22">European Journal of Human Genetics</searchLink>. Feb2014, Vol. 22 Issue 2, p286-288. 3p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=93707379 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2013.150 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 286 Titles: – TitleFull: Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Elsayed, Solaf M – PersonEntity: Name: NameFull: Heller, Raoul – PersonEntity: Name: NameFull: Thoenes, Michaela – PersonEntity: Name: NameFull: Zaki, Maha S – PersonEntity: Name: NameFull: Swan, Daniel – PersonEntity: Name: NameFull: Elsobky, Ezzat – PersonEntity: Name: NameFull: Zühlke, Christine – PersonEntity: Name: NameFull: Ebermann, Inga – PersonEntity: Name: NameFull: Nürnberg, Gudrun – PersonEntity: Name: NameFull: Nürnberg, Peter – PersonEntity: Name: NameFull: Bolz, Hanno J IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 02 Text: Feb2014 Type: published Y: 2014 Identifiers: – Type: issn-print Value: 10184813 Numbering: – Type: volume Value: 22 – Type: issue Value: 2 Titles: – TitleFull: European Journal of Human Genetics Type: main |
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