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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Shranjeno v:
Bibliografske podrobnosti
izdano v: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
Jezik:Inglês
Izdano: West Asia Organization for Cancer Prevention 2018
Teme:
Research Article
Online dostop: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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