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Hemoglobin
international journal for hemoglobin research
Volume 15, 1991 - Issue 6
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Original Article

HB Yokohama [β31(B13)LEU→PRO] Detected AS A de novo Mutation in a Yugoslavian Boy

D. Plašeska Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
L. Janković Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
A. J. Dimovski Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
,
D. Milenović Department of Pediatrics, Faculty of Medicine, 18000, Niš, Yugoslavia
,
D. Jurišić Department of Clinical Chemistry, University Hospital, Dr. O. Novosel, 41000, Zagreb, Yugoslavia
&
G. D. Efremov Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
Pages 469-476 | Received 25 Jun 1991, Accepted 06 Sep 1991, Published online: 07 Jul 2009

Citations (4)

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Read on this site (1)

A. Gürgey, C. Altay, L.-H. Gu, J. Ye. Leonova, A. Delibalta, C. Öner & T. H. J. Huisman. (1995) 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. Hemoglobin 19:3-4, pages 165-172.
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Articles from other publishers (3)

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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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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N. S. Smetanina & T.H. J. Huisman. (1996) mRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants. American Journal of Hematology 52:4, pages 258-263.
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