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. 2010 Nov 15;117(10):2883–2886. doi: 10.1182/blood-2010-07-295501

Figure 1.

Figure 1

Gain-of-function somatic KRAS mutations. (A) Cell subsets were sorted by flow cytometry and used for DNA sequencing; (B) Peripheral blood mononuclear cells (PBMCs) were lysed and used for DNA sequencing; a buccal swab was also sequenced to rule out a germline mutation. The small mutant peak seen in the buccal sample probably reflects the presence of hematopoietic cells in the cell mixture.