Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes

Interstitial deletion of chromosome 5q is the most common chromosomal abnormality in myelodysplastic syndromes. The catalogue of genes involved in the molecular pathogenesis of myelodysplastic syndromes is rapidly expanding and next-generation sequencing technology allows detection of these mutation...

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Autors principals: Fernandez-Mercado, Marta, Burns, Adam, Pellagatti, Andrea, Giagounidis, Aristoteles, Germing, Ulrich, Agirre, Xabier, Prosper, Felipe, Aul, Carlo, Killick, Sally, Wainscoat, James S., Schuh, Anna, Boultwood, Jacqueline
Format: Artigo
Idioma:Inglês
Publicat: Ferrata Storti Foundation 2013
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3856960/
https://ncbi.nlm.nih.gov/pubmed/23831921
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2013.086686
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