Identification of Novel Insertions and Deletions in Haematopoietic Stem/Progenitor Cells in de novo Myelodysplastic Syndromes

Myelodysplastic Syndromes (MDS) are clonal haematological stem cell disorders. The molecular basis of MDS is heterogeneous and the molecular mechanisms underlying biology of this complex disorder are not fully understood. Genetic variations (GVs) occur in about 90% of patients with MDS. It has been...

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Detalles Bibliográficos
Autores principales: Bandara, Manoj, Goonasekera, Hemali, Dissanayake, Vajira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2021
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800462/
https://www.ncbi.nlm.nih.gov/pubmed/35178361
http://dx.doi.org/10.22088/IJMCM.BUMS.10.3.227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800462/
https://www.ncbi.nlm.nih.gov/pubmed/35178361
http://dx.doi.org/10.22088/IJMCM.BUMS.10.3.227

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