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A chance to cut (the genome) is a chance to cure

In this issue of Blood, Antoniani et al identify an innovative genome editing approach to induce fetal hemoglobin (HbF), which may eventually lead to therapeutic strategies for ameliorating or curing sickle-cell disease (SCD) and β-thalassemia.(1)

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Detalhes bibliográficos
Publicado no:Blood
Main Authors: Montbleau, Kara E., Sankaran, Vijay G.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5921966/
https://ncbi.nlm.nih.gov/pubmed/29699995
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2018-03-839787
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