SRSF2 mutations in myelodysplasia/myeloproliferative neoplasms

Recurrent gene mutations have been described with varying frequencies in myelodysplasia (MDS) /myeloproliferative neoplasm (MPN) overlap syndromes (MMOS). Recent work has placed significant focus on understanding the role of gene lesions involving the spliceosomal machinery in leukemogeneis. SRSF2 i...

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Detalles Bibliográficos
Autores principales: Aujla, Amandeep, Linder, Katherine, Iragavarapu, Chaitanya, Karass, Michael, Liu, Delong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158887/
https://www.ncbi.nlm.nih.gov/pubmed/30275952
http://dx.doi.org/10.1186/s40364-018-0142-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158887/
https://www.ncbi.nlm.nih.gov/pubmed/30275952
http://dx.doi.org/10.1186/s40364-018-0142-y

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