地中海贫血
胎儿血红蛋白
血红蛋白病
β地中海贫血
医学
遗传学
生物
内科学
溶血性贫血
胎儿
怀孕
作者
Dun Liu,Xinhua Zhang,Lihua Yu,Ren Cai,Xiaoxia Ma,Chengguang Zheng,Yuqiu Zhou,Qiji Liu,Xiaofeng Wei,Li Lin,Tizhen Yan,Jiwei Huang,Narla Mohandas,Xiuli An,Xiangmin Xu
出处
期刊:Blood
[American Society of Hematology]
日期:2014-05-15
卷期号:124 (5): 803-811
被引量:148
标识
DOI:10.1182/blood-2014-03-561779
摘要
Key Points The prevalence of KLF1 mutations is significantly higher in a thalassemia endemic region of China than in a nonendemic region. KLF1 mutations ameliorate the clinical and hematologic features of β-thalassemia.
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