医学
地中海贫血
胎儿血红蛋白
疾病
血红蛋白病
儿科
镰状细胞性贫血
重症监护医学
内科学
怀孕
胎儿
遗传学
生物
出处
期刊:JAMA
[American Medical Association]
日期:2021-01-12
卷期号:325 (2): 121-121
被引量:3
标识
DOI:10.1001/jama.2020.26232
摘要
Genetic approaches against sickle cell disease (SCD) and transfusion-dependent β-thalassemia (TDT) increased fetal hemoglobin and appeared to improve clinical outcomes in 2 small early trials, researchers reported in the New England Journal of Medicine.
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