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Similar Publications
Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS.
Int J Lab Hematol
August 2014
Department of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.
Hb Handsworth is a rare α-globin structural variant caused by a missense mutation either on the α2 or α1-globin gene (HBA2 or HBA1: c.55G>C, p.Gly18Arg).
View Article and Find Full Text PDFThe present paper describes the structural analysis of an abnormal hemoglobin variant of alpha-chain found in a Chinese woman in the Hechi district of the Zhuang Autonomous Region of Guangxi, and finds it to be hemoglobin Handsworth (alpha 18(A16) Gly leads to Arg).
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