地中海贫血
阿尔法(金融)
α地中海贫血
血红蛋白病
医学
分子生物学
溶血性贫血
内科学
生物
遗传学
基因型
基因
外科
结构效度
患者满意度
作者
GR Honig,Mir Shamsuddin,Rina Zaizov,M Steinherz,I Solar,C Kirschmann
出处
期刊:Blood
[American Society of Hematology]
日期:1981-04-01
卷期号:57 (4): 705-711
被引量:38
标识
DOI:10.1182/blood.v57.4.705.bloodjournal574705
摘要
Tikva. a new unstable a-chain structural variant.was identified in two unrelated children whose families are from the Iraqi Jewish community of Baghdad.Both children have a-thalassemia.with hematologic features of mild HbH disease.The abnormal hemoglobin from the two patients did not separate from hemoglobin A by electrophoresis or chromatography.but the mutant a-chain emerged ahead of aA in carboxymethylcellulose column chromatography.allowing it to be isolated in pure form.Hemoglobin Petah Tikva was unstable in solution and could also be isolated by isopropanol precipitation.
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