A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β 0 0 ‐thalassaemia homozygotes

著录项

• 来源
  《British Journal of Haematology》 |2018年第5期|共3页
• 作者

  Jiang Zhihua; Luo Hong‐Yuan; Farrell John J.; Zhang Zhengjian; Schulz Vincent P.; Albarawi Dilan; Steinberg Martin H.; Al‐Allawi Nasir A.S.; Gallagher Patrick G.; Forget Bernard G.; Chui David H.K.;

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• 作者单位

  Departments of MedicineBoston University School of MedicineBoston MA USA;

  Departments of MedicineBoston University School of MedicineBoston MA USA;

  Departments of MedicineBoston University School of MedicineBoston MA USA;

  Transcription Imaging ConsortiumHoward Hughes Medical InstituteAshburn VA USA;

  Departments of Pediatrics Pathology GeneticsYale University School of MedicineNew Haven CT USA;

  Scientific Research CentreUniversity of DuhokDuhok Iraq;

  Departments of MedicineBoston University School of MedicineBoston MA USA;

  Department of Pathology and Scientific Research CentreUniversity of DuhokDuhok Iraq;

  Departments of Pediatrics Pathology GeneticsYale University School of MedicineNew Haven CT USA;

  Departments of Medicine GeneticsYale University School of MedicineNew Haven CT USA;

  Departments of MedicineBoston University School of MedicineBoston MA USA;

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• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 血液及淋巴系疾病;
• 关键词

  β‐thalassaemia; fetal haemoglobin; transcription factor; single nucleotide polymorphism;

  机译：β-地中海贫血;胎儿血红蛋白;转录因子;单核苷酸多态性;