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Sickle Cell Anemia, the First Molecular Disease: Overview of Molecular Etiology, Pathophysiology, and Therapeutic Approaches

The root cause of sickle cell disease is a single β-globin gene mutation coding for the sickle β-hemoglobin chain. Sickle hemoglobin tetramers polymerize when deoxygenated, damaging the sickle erythrocyte. A multifaceted pathophysiology, triggered by erythrocyte injury induced by the sickle hemoglob...

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Detalhes bibliográficos
Publicado no:ScientificWorldJournal
Autor principal: Steinberg, Martin H.
Formato: Artigo
Idioma:Inglês
Publicado em: TheScientificWorldJOURNAL 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5848659/
https://ncbi.nlm.nih.gov/pubmed/19112541
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1100/tsw.2008.157
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