Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India
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DOI: 10.1016/j.bjhh.2017.09.001
Abstract: Hereditary hemoglobinopathies, the most common monogenic hemoglobin (Hb) disorders, result in a variety of clinical consequences. It has been observed that various Hb variants and thalassemias are found common to specific ethnic groups and regions.… read more here.
Keywords: heterozygote diran; thalassemia; compound heterozygote; glu ... See more keywords