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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 3
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Short Communication

Identification of Three Novel Hb F Variants: Hb F-Hayward [Gγ1(NA1)Gly→Asp, GGT>GAT], Hb F-Chori-I [AγT16(A13)Gly→Asp, GGC>GAC] and Hb F-Chori-II [AγI29(B11)Gly→Glu, GGA>GAA]

Jialing CuiHemoglobinopathy Reference Laboratory, Children’s Hospital & Research Center Oakland, Oakland, California, USA
,
Christoph BaysdorferDepartment of Biology, California State University East Bay, Hayward, California, USA
,
Mahin AzimiHemoglobinopathy Reference Laboratory, Children’s Hospital & Research Center Oakland, Oakland, California, USA
,
Elliott P. VichinskyDepartment of Hematology-Oncology, Children’s Hospital & Research Center Oakland, Oakland, California, USA
&
Carolyn C. HoppeDepartment of Hematology-Oncology, Children’s Hospital & Research Center Oakland, Oakland, California, USACorrespondence[email protected]
Pages 305-309 | Received 15 Nov 2011, Accepted 24 Dec 2011, Published online: 02 Mar 2012

REFERENCES

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  • Arribalzaga K, Ricard MP, Carreno DL, Hb J-Baltimore [β16(A13)Gly→Asp] associated with β+-thalassemia in a Spanish family. Hemoglobin. 1996;20(1):79–84.
  • Schmidt RM, Bechtel KC, Johnson MH, Therrell BL Jr, Moo-Penn WF. Hemoglobin Lufkin: β29(B11)Gly→Asp. An unstable hemoglobin variant involving an internal amino acid residue. Hemoglobin. 1977;1(8):799–814.
  • So C-C, Chan AYY, Luo H-Y, Hb A2 Hong Kong – A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait. Hemoglobin. 2011;35(2):162–165.

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