The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)(0)-thalassemia commonly found in Southeast Asia

Samankaltaisia teoksia

• 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”
  Tekijä: Ghedira, Elyes Slim, et al.
  Julkaistu: (2013)
• The Molecular Basis of β-Thalassemia
  Tekijä: Thein, Swee Lay
  Julkaistu: (2013)
• Molecular basis of β thalassemia and potential therapeutic targets
  Tekijä: Thein, Swee Lay
  Julkaistu: (2017)
• Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
  Tekijä: Zhang, Jie, et al.
  Julkaistu: (2019)
• Thalassemia in Vietnamese refugees.
  Tekijä: Chaytors, R G, et al.
  Julkaistu: (1981)