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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Detalles Bibliográficos
Autores principales: Rujirachaivej, Punchita, Siriboonpiputtana, Teerapong, Rerkamnuaychoke, Budsaba, Magmuang, Suthada, Chareonsirisuthigul, Takol, Boonsakan, Paisarn, Petvises, Sawang, Sirirat, Tanasan, Niparuck, Pimjai, Chuncharunee, Suporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165635/
https://www.ncbi.nlm.nih.gov/pubmed/30049194
http://dx.doi.org/10.22034/APJCP.2018.19.7.1825

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165635/
https://www.ncbi.nlm.nih.gov/pubmed/30049194
http://dx.doi.org/10.22034/APJCP.2018.19.7.1825

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