A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family.
Saved in:
| Title: | A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family. |
|---|---|
| Authors: | Voruz, Sophie1 (AUTHOR), Noetzli, Jasmine1 (AUTHOR), Gavillet, Mathilde1 (AUTHOR), Neerman‐Arbez, Marguerite2 (AUTHOR), Rizzi, Mattia3 (AUTHOR), Alberio, Lorenzo1 (AUTHOR) Lorenzo.Alberio@chuv.ch, Casini, Alessandro4 (AUTHOR) |
| Source: | Haemophilia. Jan/Feb2026, Vol. 32 Issue 1, p344-347. 4p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 194053922 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Voruz%2C+Sophie%22">Voruz, Sophie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Noetzli%2C+Jasmine%22">Noetzli, Jasmine</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gavillet%2C+Mathilde%22">Gavillet, Mathilde</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Neerman‐Arbez%2C+Marguerite%22">Neerman‐Arbez, Marguerite</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rizzi%2C+Mattia%22">Rizzi, Mattia</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Alberio%2C+Lorenzo%22">Alberio, Lorenzo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> Lorenzo.Alberio@chuv.ch</i><br /><searchLink fieldCode="AR" term="%22Casini%2C+Alessandro%22">Casini, Alessandro</searchLink><relatesTo>4</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Haemophilia%22">Haemophilia</searchLink>. Jan/Feb2026, Vol. 32 Issue 1, p344-347. 4p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=194053922 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/hae.70185 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 344 Titles: – TitleFull: A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Voruz, Sophie – PersonEntity: Name: NameFull: Noetzli, Jasmine – PersonEntity: Name: NameFull: Gavillet, Mathilde – PersonEntity: Name: NameFull: Neerman‐Arbez, Marguerite – PersonEntity: Name: NameFull: Rizzi, Mattia – PersonEntity: Name: NameFull: Alberio, Lorenzo – PersonEntity: Name: NameFull: Casini, Alessandro IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan/Feb2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 13518216 Numbering: – Type: volume Value: 32 – Type: issue Value: 1 Titles: – TitleFull: Haemophilia Type: main |
| ResultId | 1 |