Associated Papers
Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome.
Dambietz CA et al.
Frontiers in Genetics, 2024
39233738 (PubMed )
Supplement: Table1.XLSX › Tabelle1
A novel c.82insC (p.Tyr28Leufs85X) mutation in the XK gene associated with the McLeod phenotype.
Horikawa T et al.
Transfusion, 2021
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