Association between XmnI γG-158 (C/T) gene polymorphism and Hemoglobin F level in Egyptian sickle cell disease patients
Nada Babiker Mohamed Babiker;
Abstract
Background Sickle cell disease (SCD) is a common form of hereditary disease of an autosomal recessive inheritance with a highly variable phenotype. Interindividual variation in Fetal hemoglobin (HbF) expression is a known and potentially heritable modifi
Other data
| Title | Association between XmnI γG-158 (C/T) gene polymorphism and Hemoglobin F level in Egyptian sickle cell disease patients | Other Titles | العلاقة بين تعدد الأشكال Xmn1 γG-158 (C/T) الجينية ومستوى الهيموجلوبين إفHb F في مرضى فقر الدم المنجلي المصريين | Authors | Nada Babiker Mohamed Babiker | Keywords | Association between XmnI γG-158 (C/T) gene polymorphism and Hemoglobin F level in Egyptian sickle cell disease patients | Issue Date | 2014 | Description | Background Sickle cell disease (SCD) is a common form of hereditary disease of an autosomal recessive inheritance with a highly variable phenotype. Interindividual variation in Fetal hemoglobin (HbF) expression is a known and potentially heritable modifi |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 122034R9460.pdf | 299.63 kB | Adobe PDF | View/Open |
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