Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5′δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to “The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia”

Míreanna comhchosúla

• Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5′δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to “The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia”
  de réir: Elyes Slim Ghedira, et al.
  Foilsithe / Cruthaithe: (2013-09-01)
• Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
  de réir: Jie Zhang, et al.
  Foilsithe / Cruthaithe: (2019-06-01)
• HbS-Sicilian (δβ)0-Thalassemia: A Rare Variant of Sickle Cell
  de réir: Grace Onimoe, et al.
  Foilsithe / Cruthaithe: (2017-01-01)
• JUSTIFICATION OF UNIVERSAL IRON SUPPLEMENTATION FOR INFANTS 6-12 MONTHS IN REGIONS WITH A HIGH PREVALENCE OF THALASSEMIA
  de réir: Phakatip Sinlapamongkolkul, et al.
  Foilsithe / Cruthaithe: (2023-08-01)
• Association of Xmn I Polymorphism and Hemoglobin E Haplotypes on Postnatal Gamma Globin Gene Expression in Homozygous Hemoglobin E
  de réir: Supachai Ekwattanakit, et al.
  Foilsithe / Cruthaithe: (2012-01-01)