Oxidative stress in β-thalassaemia and sickle cell disease

Sickle cell disease and β-thalassaemia are inherited haemoglobinopathies resulting in structural and quantitative changes in the β-globin chain. These changes lead to instability of the generated haemoglobin or to globin chain imbalance, which in turn impact the oxidative environment both intracellu...

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Detalles Bibliográficos
Autores principales: Voskou, S., Aslan, M., Fanis, P., Phylactides, M., Kleanthous, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543215/
https://www.ncbi.nlm.nih.gov/pubmed/26285072
http://dx.doi.org/10.1016/j.redox.2015.07.018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543215/
https://www.ncbi.nlm.nih.gov/pubmed/26285072
http://dx.doi.org/10.1016/j.redox.2015.07.018

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