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The exon A (C77G) mutation is...
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The exon A (C77G) mutation is a common cause of abnormal CD45 splicing in humans
Show other versions (1)
Manylion Llyfryddiaeth
Prif Awduron:
Tchilian, E
,
Wallace, D
,
Imami, N
,
Liao, H
,
Burton, C
,
Gotch, F
,
Martinson, J
,
Haynes, B
,
Beverley, P
Fformat:
Journal article
Cyhoeddwyd:
2001
Daliadau
Disgrifiad
Other Versions (1)
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
The exon A (C77G) mutation is a common cause of abnormal CD45 splicing in humans.
gan: Tchilian, E, et al.
Cyhoeddwyd: (2001)
A point mutation in CD45 may be associated with an increased risk of HIV-1 infection.
gan: Tchilian, E, et al.
Cyhoeddwyd: (2001)
A point mutation in CD45 may be associated with an increased risk of HIV-1 infection
gan: Tchilian, E, et al.
Cyhoeddwyd: (2001)
Novel perforin mutation in a patient with hemophagocytic lymphohistiocytosis and CD45 abnormal splicing.
gan: McCormick, J, et al.
Cyhoeddwyd: (2003)
Novel perforin mutation in a patient with hemophagocytic lymphohistiocytosis and CD45 abnormal splicing
gan: McCormick, J, et al.
Cyhoeddwyd: (2003)