Patients with XLP type 1 have variable numbers of NKT cells

Summary X‐linked lymphoproliferative disease (XLP1) is a rare primary immunodeficiency that usually presents in early childhood. Patients with XLP1 have been reported to have absent NKT cells, and it has been suggested that this can be diagnostic for the disorder. Whilst NKT frequency in adults is v...

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Veröffentlicht in:British journal of haematology 2022-07, Vol.198 (1), p.151-154
Hauptverfasser: Ralph, Elizabeth, Evans, Josie, Booth, Claire, Gilmour, Kimberly
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Sprache:eng
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