A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome
| Title: | A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome |
|---|---|
| Authors: | Al-Numair, Nouf, Ramzan, Khushnooda, Alquait, Laila, Alshehri, Meshal, Imtiaz, Faiqa, Owaidah, Tarek |
| Source: | Blood coagulation and fibrinolysis. 32(5):352-355 |
| Availability: | http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122529566.0x000001&indx=1&recIds=ETOCvdc_100122529566.0x000001 |
| Database: | British Library Document Supply Centre Inside Serials & Conference Proceedings |
| FullText | Text: Availability: 0 CustomLinks: – Url: https://resolver.ebsco.com/c/xy5jbn/result?sid=EBSCO:edsbl&genre=article&issn=09575235&ISBN=&volume=32&issue=5&date=20210101&spage=352&pages=352-355&title=Blood coagulation and fibrinolysis&atitle=A%20homozygous%20loss-of-function%20mutation%20in%20GP1BB%20causing%20variable%20clinical%20phenotypes%20in%20a%20family%20with%20Bernard%E2%80%93Soulier%20syndrome&aulast=Al-Numair%2C%20Nouf&id=DOI: Name: Full Text Finder (for New FTF UI) (s8985755) Category: fullText Text: Find It @ SCU Libraries MouseOverText: Find It @ SCU Libraries |
|---|---|
| Header | DbId: edsbl DbLabel: British Library Document Supply Centre Inside Serials & Conference Proceedings An: vdc.100122529566.0x000001 RelevancyScore: 909 AccessLevel: 2 PubType: Periodical PubTypeId: serialPeriodical PreciseRelevancyScore: 909.003845214844 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Al-Numair%2C+Nouf%22">Al-Numair, Nouf</searchLink><br /><searchLink fieldCode="AR" term="%22Ramzan%2C+Khushnooda%22">Ramzan, Khushnooda</searchLink><br /><searchLink fieldCode="AR" term="%22Alquait%2C+Laila%22">Alquait, Laila</searchLink><br /><searchLink fieldCode="AR" term="%22Alshehri%2C+Meshal%22">Alshehri, Meshal</searchLink><br /><searchLink fieldCode="AR" term="%22Imtiaz%2C+Faiqa%22">Imtiaz, Faiqa</searchLink><br /><searchLink fieldCode="AR" term="%22Owaidah%2C+Tarek%22">Owaidah, Tarek</searchLink> – Name: TitleSource Label: Source Group: Src Data: <i>Blood coagulation and fibrinolysis</i>. 32(5):352-355 – Name: URL Label: Availability Group: URL Data: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122529566.0x000001&indx=1&recIds=ETOCvdc_100122529566.0x000001 |
| PLink | https://login.libproxy.scu.edu/login?url=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsbl&AN=vdc.100122529566.0x000001 |
| RecordInfo | BibRecord: BibEntity: Languages: – Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 352 Titles: – TitleFull: A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Al-Numair, Nouf – PersonEntity: Name: NameFull: Ramzan, Khushnooda – PersonEntity: Name: NameFull: Alquait, Laila – PersonEntity: Name: NameFull: Alshehri, Meshal – PersonEntity: Name: NameFull: Imtiaz, Faiqa – PersonEntity: Name: NameFull: Owaidah, Tarek IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 09575235 – Type: issn-locals Value: edsbl.Periodical Numbering: – Type: volume Value: 32 – Type: issue Value: 5 Titles: – TitleFull: Blood coagulation and fibrinolysis Type: main |
| ResultId | 1 |