SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency.
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| Title: | SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency. |
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| Authors: | Ruf, Maximilian1 (AUTHOR), Cunningham, Sarah1 (AUTHOR), Wandersee, Alexandra1 (AUTHOR), Brox, Regine1 (AUTHOR), Achenbach, Susanne1 (AUTHOR), Strobel, Julian1 (AUTHOR), Hackstein, Holger1 (AUTHOR), Schneider, Sabine1 (AUTHOR) sabine.schneider@uk-erlangen.de |
| Source: | Thrombosis Journal. 2/12/2024, Vol. 22 Issue 1, p1-11. 11p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 175389792 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ruf%2C+Maximilian%22">Ruf, Maximilian</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cunningham%2C+Sarah%22">Cunningham, Sarah</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wandersee%2C+Alexandra%22">Wandersee, Alexandra</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Brox%2C+Regine%22">Brox, Regine</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Achenbach%2C+Susanne%22">Achenbach, Susanne</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Strobel%2C+Julian%22">Strobel, Julian</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hackstein%2C+Holger%22">Hackstein, Holger</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schneider%2C+Sabine%22">Schneider, Sabine</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> sabine.schneider@uk-erlangen.de</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Thrombosis+Journal%22">Thrombosis Journal</searchLink>. 2/12/2024, Vol. 22 Issue 1, p1-11. 11p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=175389792 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12959-024-00589-5 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ruf, Maximilian – PersonEntity: Name: NameFull: Cunningham, Sarah – PersonEntity: Name: NameFull: Wandersee, Alexandra – PersonEntity: Name: NameFull: Brox, Regine – PersonEntity: Name: NameFull: Achenbach, Susanne – PersonEntity: Name: NameFull: Strobel, Julian – PersonEntity: Name: NameFull: Hackstein, Holger – PersonEntity: Name: NameFull: Schneider, Sabine IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 02 Text: 2/12/2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 14779560 Numbering: – Type: volume Value: 22 – Type: issue Value: 1 Titles: – TitleFull: Thrombosis Journal Type: main |
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