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Article

The Frequency of SF3B1 Mutations in Thai Patients with Myelodysplastic Syndrome

Asian Pacific journal of cancer prevention : APJCP - 27 Jul 2018

Rujirachaivej Punchita, Siriboonpiputtana Teerapong, Rerkamnuaychoke Budsaba, Magmuang Suthada, Chareonsirisuthigul Takol, Boonsakan Paisarn, Petvises Sawang, Sirirat Tanasan, Niparuck Pimjai, Chuncharunee Suporn

Abstract excerpt

Genetic mutations in genes encoding critical component of RNA splicing machinery including SF3B1 are frequently identified and recognized as the pathogenesis in the development of myelodysplatic syndrome (MDS). In this study, PCR sequencings specific for SF3B1 exon 13, 14, 15, and 16 were performed to analyse genomic DNA isolated from bone marrow samples of 72 newly diagnosed MDS patients. We found that 10 of 72...

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Identifiers

PMID: 30049194
DOI: 10.22034/APJCP.2018.19.7.1825
PMCID: PMC6165635

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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