Compound heterozygosity for α thalassemia-2 and hemoglobin seal rock produces mild Hb H disease: The α-globin chain mutation in Hb seal rock is a TAA→GAA transversion in the termination codon of the 5′ α2-globin gene
M. Coleman, V. Fairbanks, D. Merritt, G. Rodgers, S. Thibodeau, M. Steinberg, R. Jones
Research output: Contribution to journal › Article › peer-review
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