Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor

Sickle Cell Disease (SCD) is a monogenic hereditary blood disorder caused by a single point mutation (β(S)) in the β globin gene resulting in an abnormal hemoglobin (HbS) that can polymerize within the erythrocytes, inducing their characteristic sickle shape. This causes hemolytic anemia and occlusi...

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Detalles Bibliográficos
Autores principales: Breveglieri, Giulia, D’Aversa, Elisabetta, Cosenza, Lucia Carmela, Boutou, Effrossyni, Balassopoulou, Angeliki, Voskaridou, Ersi, Gambari, Roberto, Borgatti, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Sequoia 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894342/
https://www.ncbi.nlm.nih.gov/pubmed/31853166
http://dx.doi.org/10.1016/j.snb.2019.05.081

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894342/
https://www.ncbi.nlm.nih.gov/pubmed/31853166
http://dx.doi.org/10.1016/j.snb.2019.05.081

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