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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 3-4
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Original Article

HB Hakkari or α2β231(B13)LEU→ARG, A Severely Unstable Hemoglobin Variant Associated with Numerous Intra-Erythroblastic Inclusions and Erythroid Hyperplasia of the Bone Marrow

A. Gürgey Department of Pediatrics, Children's Medical Center Hacettepe University, Ankara, Turkey
,
C. Altay Department of Pediatrics, Children's Medical Center Hacettepe University, Ankara, Turkey
,
L.-H. Gu Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. Ye. Leonova Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
A. Delibalta Pediatrician, Hakkari, Turkey
,
C. Öner Department of Pediatrics, Children's Medical Center Hacettepe University, Ankara, Turkey
&
T. H. J. Huisman Laboratory of Protein Chemistry and Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
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Pages 165-172 | Received 03 Oct 1994, Accepted 03 Mar 1995, Published online: 07 Jul 2009

Citations (6)

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Read on this site (2)

M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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Articles from other publishers (4)

S. G. Mann, M. V. Krasilnikova, N. A. Karamjan, M. E. Lokhmatova, A. O. Koposova, E. A. Litvin & S. A. Plyasunova. (2022) Rare unstable hemoglobin Hakkari in Russia: a case report and literature review. Pediatric Hematology/Oncology and Immunopathology 21:3, pages 77-83.
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Sushmita Nair, Lamis K Eldjerou, Neil S. Harris & Levette N. Dunbar. (2014) Rare form of autosomal dominant thalassemia-Hemoglobin Hakkari. Pediatric Blood & Cancer 61:11, pages 2118-2120.
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Hernan Sabio, Natalia Dixon, Niren Patel, Chinwe Obiaga, Lina Zhuang, Steffen E. Meiler, Abdullah Kutlar & Ferdane Kutlar. (2011) Thalassemia-like Phenotype in a Novel Complex Hemoglobinopathy With α, β, δ Globin Chain Abnormalities. Journal of Pediatric Hematology/Oncology 33:8, pages 589-591.
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B. Kanathezhath, F.K. Hazard, H. Guo, J. Kidd, M. Azimi, F.A. Kuypers, E.P. Vichinsky & A. Lal. (2010) Hemoglobin Hakkari: An autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. Pediatric Blood & Cancer 54:2, pages 332-335.
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