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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Pharmgenomics Pers Med
Egile Nagusiak: Husain, Marium, Hartman, Amber D, Desai, Payal
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Dove Medical Press 2017
Gaiak:
Sarrera elektronikoa: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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