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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Enregistré dans:
Détails bibliographiques
Publié dans:Asian Pac J Cancer Prev
Auteurs principaux: Rujirachaivej, Punchita, Siriboonpiputtana, Teerapong, Rerkamnuaychoke, Budsaba, Magmuang, Suthada, Chareonsirisuthigul, Takol, Boonsakan, Paisarn, Petvises, Sawang, Sirirat, Tanasan, Niparuck, Pimjai, Chuncharunee, Suporn
Format: Artigo
Langue:Inglês
Publié: West Asia Organization for Cancer Prevention 2018
Sujets:
Research Article
Accès en ligne: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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