地中海贫血
遗传诊断
疾病
遗传增强
β地中海贫血
遗传学
生物
中国
医学
基因
内科学
历史
考古
作者
Jingzhi Zhang,Jingbin Yan,Fanyi Zeng
摘要
Thalassemia is a recessive monogenic hematological disease associated with reduced amounts of functional hemoglobin caused by mutations/deletions in at least one of the globin genes. This disease has attracted significant attention throughout the years in terms of genetic diagnosis and developments in gene and cell therapy. Here, recent progress is reviewed in the genetic diagnosis and development of therapeutics for thalassemia, particularly β-thalassemia, in China and around the world.
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