2087

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a family of inherited disorders of hemoglobin synthesis characterized by a reduced output of one or other of the globin chains of adult hemoglobin. The thalassemias are classified, according to the particular globin chain that is ineffectively produced, as the a , b , db and gdb thalassemias. The a and b thalassemias are by far the most important. It is a kind of hereditary hemolytic anemia, wh...

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ژورنال

عنوان ژورنال: Journal of Clinical and Translational Science

سال: 2017

ISSN: 2059-8661

DOI: 10.1017/cts.2017.243