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.
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
Description
ISSN:1664-8021
DOI:10.3389/fgene.2024.1421952