Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China

مواد مشابهة

• The prevalence and molecular characterization of (δβ)(0)‐thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population
  بواسطة: He, Sheng, وآخرون
  منشور في: (2017)
• Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China
  بواسطة: Jiang, Fan, وآخرون
  منشور في: (2020)
• Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs
  بواسطة: Fornari, Thais A, وآخرون
  منشور في: (2016)
• 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”
  بواسطة: Ghedira, Elyes Slim, وآخرون
  منشور في: (2013)
• Induction of Fetal Hemoglobin by Introducing Natural Hereditary Persistence of Fetal Hemoglobin Mutations in the γ-Globin Gene Promoters for Genome Editing Therapies for β-Thalassemia
  بواسطة: Dian Lu, وآخرون
  منشور في: (2022-05-01)