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BioMed Research International
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2014
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Article
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Fig 2
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Research Article
MYD88 L265P Mutations Are Correlated with 6q Deletion in Korean Patients with Waldenström Macroglobulinemia
Figure 2
Somatic mutations of MYD88 L265P found in 11 Waldenström macroglobulinemia patients by Sanger sequencing method.