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

A Newly Discovered β°-Thalassemia (IVS-11-850, G→A) Mutation in a North European Family

M. A. Çürük Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
S. C. Howard Monsanto, Inc., St Louis, MO, 63167, USA
,
A. Kutlar Department of Medicine, Medical College of Georgia, Augusta, GA, 30912-3125, USA
&
T. H. J. Huisman Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 207-211 | Received 03 Jan 1995, Accepted 31 Jan 1995, Published online: 07 Jul 2009

Citations (6)

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Read on this site (3)

Fan Jiang, Gui-Lan Chen, Jian-Ying Zhou & Dong-Zhi Li. (2017) First Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese Family. Hemoglobin 41:4-6, pages 286-287.
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John S. Waye, Barry Eng, Laurie Hellens, Betty-Ann Hohenadel, Lisa M. Nakamura & Lynda Walker. (2013) Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A). Hemoglobin 37:4, pages 378-386.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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Articles from other publishers (3)

Riham H.N. AlMosawi, Nihad A.M. Al-Rashedi & Najla I. Ayoub. (2020) Clinical Laboratory Manifestation and Molecular Diagnosis of β-Thalassemia Patients in Iraq. Journal of Pediatric Hematology/Oncology 42:1, pages 27-31.
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M. Knott, K.M.A. Ramadan, G. Savage, F.G.C. Jones, M. El-Agnaf, M.F. McMullin & M.J. Percy. (2006) Novel and Mediterranean β thalassemia mutations in the indigenous Northern Ireland population. Blood Cells, Molecules, and Diseases 36:2, pages 265-268.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .

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