Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome.
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| Title: | Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome. |
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| Authors: | Dambietz CA; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany., Doescher A; DRK Blutspendedienst NSTOB, Institute Bremen-Oldenburg, Springe, Germany., Heming M; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany., Schirmacher A; Central Laboratory, University Hospital Münster, Münster, Germany., Schlüter B; Central Laboratory, University Hospital Münster, Münster, Germany., Schulte-Mecklenbeck A; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany., Thomas C; Institute of Neuropathology, University Hospital Münster and University of Münster, Münster, Germany., Wiendl H; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany., Meyer Zu Hörste G; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany., Wiethoff S; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany. |
| Source: | Frontiers in genetics [Front Genet] 2024 Aug 21; Vol. 15, pp. 1421952. Date of Electronic Publication: 2024 Aug 21 (Print Publication: 2024). |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39233738 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Dambietz+CA%22">Dambietz CA</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Doescher+A%22">Doescher A</searchLink>; DRK Blutspendedienst NSTOB, Institute Bremen-Oldenburg, Springe, Germany.<br /><searchLink fieldCode="AU" term="%22Heming+M%22">Heming M</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Schirmacher+A%22">Schirmacher A</searchLink>; Central Laboratory, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Schlüter+B%22">Schlüter B</searchLink>; Central Laboratory, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Schulte-Mecklenbeck+A%22">Schulte-Mecklenbeck A</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Thomas+C%22">Thomas C</searchLink>; Institute of Neuropathology, University Hospital Münster and University of Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Wiendl+H%22">Wiendl H</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Meyer+Zu+Hörste+G%22">Meyer Zu Hörste G</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Wiethoff+S%22">Wiethoff S</searchLink>; Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2024 Aug 21; Vol. 15, pp. 1421952. <i>Date of Electronic Publication: </i>2024 Aug 21 (<i>Print Publication: </i>2024). – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39233738 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fgene.2024.1421952 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1421952 Titles: – TitleFull: Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dambietz CA – PersonEntity: Name: NameFull: Doescher A – PersonEntity: Name: NameFull: Heming M – PersonEntity: Name: NameFull: Schirmacher A – PersonEntity: Name: NameFull: Schlüter B – PersonEntity: Name: NameFull: Schulte-Mecklenbeck A – PersonEntity: Name: NameFull: Thomas C – PersonEntity: Name: NameFull: Wiendl H – PersonEntity: Name: NameFull: Meyer Zu Hörste G – PersonEntity: Name: NameFull: Wiethoff S IsPartOfRelationships: – BibEntity: Dates: – D: 21 M: 08 Text: 2024 Aug 21 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 1664-8021 Numbering: – Type: volume Value: 15 Titles: – TitleFull: Frontiers in genetics Type: main |
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