A carregar...
Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients
BACKGROUND: β-thalassemia is the most common monogenic disorder in human. The (CT) polymorphism at -158 upstream region of the γ(G)-globin gene and pharmacological factors such as hydroxyurea have been reported to influence γ-globin gene expression and the severity of clinical symptoms of β-thalasse...
Na minha lista:
| Publicado no: | Iran Biomed J |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pasteur Institute of Iran
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4571014/ https://ncbi.nlm.nih.gov/pubmed/26024726 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7508/ibj.2015.03.008 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|