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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Haemoglobin H disease due to (--SEA) alpha-globin gene deletion and alpha2-codon 30 (DeltaGAG) mutation: a family

S K Ma1, A Y Chan, E K Chiu

  • 1Haematology Section, Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong, China. eskma@hkucc.hku.hk

Clinical and Laboratory Haematology
|November 13, 2001
PubMed

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