Highly Influential Citations2
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Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a rare hemoglobin (Hb) variant due to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid substitution. Two… Continue Reading
Introduction: Hemoglobin Constant Spring (HbCS) is often missed due to almost normal red cells indices and is present at a low level in peripheral blood. However, analysis of blood samples using… Continue Reading
Abstract This multiple-case study drew upon Engestrom's (1987) activity theory (AT) to understand the conditions and explain the systematic contradictions that facilitate successful Information and… Continue Reading
Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice site mutation interferes with normal… Continue Reading