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Pharmacogenomics of sickle cell disease: steps toward personalized medicine

Sickle cell disease (SCD) is a monogenetic disease but has a wide range of phenotypic expressions. Some of these differences in phenotype can be explained by genetic polymorphisms in the human globin gene. These polymorphisms can result in different responses to typical treatment, sometimes leading...

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Detalles Bibliográficos
Autores principales: Husain, Marium, Hartman, Amber D, Desai, Payal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656342/
https://www.ncbi.nlm.nih.gov/pubmed/29089781
http://dx.doi.org/10.2147/PGPM.S123427