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. 2018 Jul 19;32(12):2617–2625. doi: 10.1038/s41375-018-0197-7

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — AS-PCR and Sanger sequencing for MYD88 L265P in tDNA and cfDNA. WM1 and WM2 present in both wild-type and mutant products, while WM displays oonly the wild-type allele. WM1 and WM3 cfDNA sequencing analysis is also displayed