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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Detaylı Bibliyografya
Yayımlandı:Asian Pac J Cancer Prev
Asıl Yazarlar: Rujirachaivej, Punchita, Siriboonpiputtana, Teerapong, Rerkamnuaychoke, Budsaba, Magmuang, Suthada, Chareonsirisuthigul, Takol, Boonsakan, Paisarn, Petvises, Sawang, Sirirat, Tanasan, Niparuck, Pimjai, Chuncharunee, Suporn
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: West Asia Organization for Cancer Prevention 2018
Konular:
Research Article
Online Erişim: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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