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Acknowledgments
All the samples were from Jiangsu Biobank of Clinical Resources.
Funding
This study was supported by grant from the National Key R&D Program of China (2019YFA0111000), the National Natural Science Foundation of China (81,570,138, 81,570,139, 81,600,116, 81,600,114, 81,700,140, 81,873,449, 81,970,142, 81,900,130, 81,970,136), the Natural Science Foundation of the Jiangsu Higher Education Institution of China (18KJA320005), the Natural Science Foundation of Jiangsu Province (BK20190180), China Postdoctoral Science Foundation (2018 M632372), the priority academic program development of Jiangsu Higher Education Institution, the Innovation Capability Development Project of Jiangsu Province (BM2015004), and National Science and Technology Major Project (2017ZX09304021).
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XFY designed this study. XFY and LM wrote the paper; LZ and MW analyzed RNA-seq data and designed primers; ZW and ZZ collected samples and clinical data; LJW, YX, LM, LY and JNC performed RT-PCR and Sanger sequencing; HZL, JLP, ANS, SNC and DPW gave advice for the study design and paper writing.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the First Affiliated Hospital of Soochow University committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
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Informed consent was obtained from all individual participants included in the study.
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Zhang, L., Wang, M., Wang, Z. et al. Identification of a novel ETV6 truncated fusion gene in myeloproliferative neoplasm, unclassifiable with t(4;12)(q12;p13). Ann Hematol 99, 2445–2447 (2020). https://doi.org/10.1007/s00277-020-04207-y
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DOI: https://doi.org/10.1007/s00277-020-04207-y