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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: West Asia Organization for Cancer Prevention 2018
Assuntos:
Research Article
Acesso em linha: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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