The XmnI andBCL11ASingle Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients-Reference-Cited by-同舟云学术

The XmnI andBCL11ASingle Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients

Published:2012-06-11 Issue:4 Volume:36 Page:371-380
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Banan Mehdi,Bayat Hadi,Azarkeivan Azita,Mohammadparast Saeid,Kamali Koorosh,Farashi Samaneh,Bayat Nooshin,Khani Masumeh Hadavand,Neishabury Maryam,Najmabadi Hossein

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.691147

Reference34 articles.

1. Fetal hemoglobin chemical inducers for treatment of hemoglobinopathies

2. Induction of Fetal Hemoglobin in the Treatment of Sickle Cell Disease and β Thalassemia

3. Systematic Review: Hydroxyurea for the Treatment of Adults with Sickle Cell Disease

4. Acquired DNA mutations associated with in vivo hydroxyurea exposure

5. Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

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