Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype.

IF 1.2 4区医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Hemoglobin Pub Date : 2025-01-13 DOI:10.1080/03630269.2024.2449450

Ajmeera A Azeez, Prashant Sharma, Jasbir Kaur Hira, Deepak Bansal

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非输血依赖型地中海贫血患儿中共存β-地中海贫血性状、吉尔伯特综合征和α -珠蛋白基因三倍

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来源期刊

Hemoglobin 医学-生化与分子生物学

CiteScore

1.70

自引率

10.00%

发文量

审稿时长

3 months

期刊介绍： Hemoglobin is a journal in the English language for the communication of research and information concerning hemoglobin in humans and other species. Hemoglobin publishes articles, reviews, points of view The journal covers topics such as: structure, function, genetics and evolution of hemoglobins biochemical and biophysical properties of hemoglobin molecules characterization of hemoglobin disorders (variants and thalassemias), consequences and treatment of hemoglobin disorders epidemiology and prevention of hemoglobin disorders (neo-natal and adult screening) modulating factors methodology used for diagnosis of hemoglobin disorders

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