The exon A (C77G) mutation is a common cause of abnormal CD45 splicing in humans
Egile Nagusiak: | Tchilian, E, Wallace, D, Imami, N, Liao, H, Burton, C, Gotch, F, Martinson, J, Haynes, B, Beverley, P |
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Formatua: | Journal article |
Argitaratua: |
2001
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Antzeko izenburuak
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The exon A (C77G) mutation is a common cause of abnormal CD45 splicing in humans.
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A point mutation in CD45 may be associated with an increased risk of HIV-1 infection
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Novel perforin mutation in a patient with hemophagocytic lymphohistiocytosis and CD45 abnormal splicing
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