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

• Hauptverfasser: Fan Jiang (Verfasst von), Liandong Zuo (Verfasst von), Dongzhi Li (Verfasst von), Jian Li (Verfasst von), Xuewei Tang (Verfasst von), Guilan Chen (Verfasst von), Jianying Zhou (Verfasst von), Hang Lu (Verfasst von), Can Liao (Verfasst von)
• Format: Buch
• Veröffentlicht: BMC, 2020-02-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: Connect to this object online.

Abstract Background Individuals with δβ-thalassemia/HPFH and β-thalassemia usually present with intermedia or thalassemia major. No large-scale survey on HPFH/δβ-thalassemia in southern China has been reported to date. The purpose of this study was to examine the molecular epidemiology and hematolog...