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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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| Pubblicato in: | Pharmgenomics Pers Med |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Dove Medical Press
2017
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| Soggetti: | |
| Accesso online: | 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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