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Therapeutic strategies for sickle cell disease: towards a multi-agent approach

For over 100 years, clinicians and scientists have been unraveling the consequences of the A to T substitution in the beta globin gene that produces hemoglobin S, which leads to the systemic manifestations of sickle cell disease (SCD), including vaso-occlusion, anemia, hemolysis, organ injury and pa...

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Detalhes bibliográficos
Publicado no:Nat Rev Drug Discov
Main Authors: Telen, Marilyn J., Malik, Punam, Vercellotti, Gregory M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6645400/
https://ncbi.nlm.nih.gov/pubmed/30514970
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41573-018-0003-2
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