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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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Опубликовано в: :Pharmgenomics Pers Med
Главные авторы: Husain, Marium, Hartman, Amber D, Desai, Payal
Формат: Artigo
Язык:Inglês
Опубликовано: Dove Medical Press 2017
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5656342/
https://ncbi.nlm.nih.gov/pubmed/29089781
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PGPM.S123427
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