Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease: An Update on Management

The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of the β globin gene resulting in the substitution of glutamic acid by valine at position 6 of the β globin polypeptide chain. Although the molecular lesion is a single-point mutation, the sickle gene is plei...

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Detalles Bibliográficos
Autores principales: Ballas, Samir K., Kesen, Muge R., Goldberg, Morton F., Lutty, Gerard A., Dampier, Carlton, Osunkwo, Ifeyinwa, Wang, Winfred C., Hoppe, Carolyn, Hagar, Ward, Darbari, Deepika S., Malik, Punam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific World Journal 2012
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415156/
https://www.ncbi.nlm.nih.gov/pubmed/22924029
http://dx.doi.org/10.1100/2012/949535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415156/
https://www.ncbi.nlm.nih.gov/pubmed/22924029
http://dx.doi.org/10.1100/2012/949535

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