Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania
BACKGROUND: Fetal hemoglobin (HbF) is an important modulator of sickle cell disease (SCD). HbF has previously been shown to be affected by variants at three loci on chromosomes 2, 6 and 11, but it is likely that additional loci remain to be discovered. METHODS AND FINDINGS: We conducted a genome-wid...
Κύριοι συγγραφείς: | Mtatiro, SN, Singh, T, Rooks, H, Mgaya, J, Mariki, H, Soka, D, Mmbando, B, Msaki, E, Kolder, I, Thein, S, Menzel, S, Cox, SE, Makani, J, Barrett, J |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
Public Library of Science
2014
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
ανά: Siana Nkya Mtatiro, κ.ά.
Έκδοση: (2014-01-01) -
High prevalence of individuals with low concentration of fetal hemoglobin in F-cells in sickle cell anemia in Tanzania.
ανά: Urio, F, κ.ά.
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Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
ανά: Makani, J, κ.ά.
Έκδοση: (2011) -
Fetal hemoglobin is associated with peripheral oxygen saturation in sickle cell disease in Tanzania.
ανά: Nkya, S, κ.ά.
Έκδοση: (2017) -
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
ανά: Siana Nkya, κ.ά.
Έκδοση: (2017-09-01)