beta-thalassemia是什么意思、beta-thalassemia怎么读 读音:美[´biːtəθəlɑːs´iːmiə]英[´biːtəθəlɑːs´iːmiə] 英汉翻译近义词典英英词典发音词典 beta-thalassemia中文翻译 n.β型地中海贫血 beta-thalassemia是什么意思 ...
beta-thalassemia [英]'bi:təθəlɑ:s'i:mɪə [美]'bi:təθəlɑ:s'i:mɪr [医]β-地中海贫血 [例句]Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children. β-地中海贫血;造血干细胞移植;单倍体;儿童. 手机提问的朋友在客户端右上角...
β地中海贫血(beta-Thalassemia) 胎儿血红蛋白(Fetal Hemoglobin) 电泳(Electrophoresis) 年龄组(Age Groups) 醋酸(Acetic Aci…new.med.wanfangdata.com.cn|基于37个网页 3. 地中海贫血症 β-地中海贫血症(beta-thalassemia)是一种遗传性疾病,是由于编码β珠蛋白(beta-globin)的基因存在缺陷造成的。所以血红蛋白中...
Emily Mullin,WIRED, 10 July 2023All eyes right now are on exa-cel, a gene-editing therapy that awaits regulatory approvals for use in two conditions — sickle cell disease and transfusion-dependentbeta-thalassemia.— The Motley Fool,Dallas News, 10 May 2023Other licensed gene therapies, like ...
Beta-thalassemia (β-thalassemia) is a form of thalassemia due to mutations in the HBB gene on chromosome 11, inherited in an autosomal recessive fashion. The severity of the disease depends on the nature of the mutation. Alleles without a mutation that reduces function are characterized as (...
Beta-thalassemia (β-thalassemia) is an autosomal recessive disorder caused by point mutations, insertions, and deletions in the HBB gene cluster, resu
beta-thalassemia [英]'bi:təθəlɑ:s'i:mɪə[美]'bi:təθəlɑ:s'i:mɪr [医]β-地中海贫血 [例句]Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children.β-地中海贫血；造血干细胞移植；单倍体；儿童。
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at ...
Beta-thalassemia (β-thalassemia) is characterized by reduced synthesis of the hemoglobin subunit beta (hemoglobin beta chain) that results in microcytic hypochromic anemia, an abnormal peripheral blood smear with nucleated red blood cells, and reduced amounts of hemoglobin A (HbA) on hemoglobin analy...
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at ...