The Frequency of SF3B1 Mutations in Thai Patients with Myelodysplastic Syndrome

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...

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Bibliografiske detaljer
Udgivet i:Asian Pac J Cancer Prev
Main Authors: Rujirachaivej, Punchita, Siriboonpiputtana, Teerapong, Rerkamnuaychoke, Budsaba, Magmuang, Suthada, Chareonsirisuthigul, Takol, Boonsakan, Paisarn, Petvises, Sawang, Sirirat, Tanasan, Niparuck, Pimjai, Chuncharunee, Suporn
Format: Artigo
Sprog:Inglês
Udgivet: West Asia Organization for Cancer Prevention 2018
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6165635/
https://ncbi.nlm.nih.gov/pubmed/30049194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22034/APJCP.2018.19.7.1825
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