突变
中国
医学
遗传学
内科学
儿科
生物
基因
历史
考古
作者
Xiaohua Yu,Yi-Yuan Ge,Xiaomin Ma,Guang-Kuan Zeng,Yuwei Liao,Lili Liu,Yan-Bin Cao,Jian-Lian Liang,Bai-ru Lai,Yan-Qing Zeng,Yu-Chan Huang,Li‐Ye Yang
出处
期刊:Hematology
[Maney Publishing]
日期:2024-11-12
卷期号:29 (1): 2426829-2426829
标识
DOI:10.1080/16078454.2024.2426829
摘要
HbA2: c.96-2A > G mutation carriers exhibit the phenotype of α-thalassemia, and when the HbA2:c.96-2A > G mutation is combined with - SEA deletion, an intermediate phenotype of anemia is produced.
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