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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 5-6
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Original Article

Homozygous βd`-39 Mutation with Thalassemia Intermedia in Northern Sardinia: Clinical, Hematological and Molecular Analysis

L. Oggiano Chair of Hematology, Institute of Clinical Medicine L.I.T.E.F., University of Sassari, Sassari, Italy
,
F. Dore Chair of Hematology, Institute of Clinical Medicine L.I.T.E.F., University of Sassari, Sassari, Italy
,
P. Pistidda National Research Council, Laboratory for Mediterranean Anemies, Cagliari and Sassari, Italy
,
L. Guiso National Research Council, Laboratory for Mediterranean Anemies, Cagliari and Sassari, Italy
,
L. Manca Institute of General Physiology and Biochemistry L.I.T.E.F., University of Sassari, Sassari, Italy
,
B. Masala Institute of General Physiology and Biochemistry L.I.T.E.F., University of Sassari, Sassari, Italy
,
M. Pirastu National Research Council, Laboratory for Mediterranean Anemies, Cagliari and Sassari, Italy
,
C. Rosatelli Institute of Clinic and Biology of Developmental Age University of Cagliari, Cagliari, Italy
,
A. Cao Institute of Clinic and Biology of Developmental Age University of Cagliari, Cagliari, Italy
&
M. Longinotti Chair of Hematology, Institute of Clinical Medicine L.I.T.E.F., University of Sassari, Sassari, Italy
 show all
Pages 673-680 | Received 19 Oct 1987, Accepted 07 Jun 1988, Published online: 07 Jul 2009

Citations (12)

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C. Vrettou, E. Kanavakis, J. Traeger-Synodinos, A. Metaxotou-Mavrommati, I. Basiakos, E. Maragoudaki, A. Stamoulakatou, I. Papassotiriou & C. Kattamis. (2000) Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels. Hemoglobin 24:3, pages 203-220.
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S. El-Kalla & A. R. Mathews. (1997) A Significant β-Thalassemia Heterogeneity in the United Arab Emirates. Hemoglobin 21:3, pages 237-247.
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Bruno Masala. (1992) Hemoglobinopathies in Sardinia. Hemoglobin 16:4, pages 331-351.
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X-J. Wen & S. Liang. (1992) Mild HB Constant Spring-HB H Disease with β°-Thalassemia Trait. Hemoglobin 16:4, pages 321-323.
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S. A. Liebhaber. (1989) α Thalassemia. Hemoglobin 13:7-8, pages 685-731.
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Articles from other publishers (7)

Sachith Mettananda, Richard J. GibbonsDouglas R. Higgs. (2015) α-Globin as a molecular target in the treatment of β-thalassemia. Blood 125:24, pages 3694-3701.
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Alessandra Falchi, Laurianne Giovannoni, Lucia Vacca, Veronica Latini, Giuseppe Vona & Laurent Varesi. (2005) ?-globin gene cluster haplotypes associated with ?-thalassemia on Corsica island. American Journal of Hematology 78:1, pages 27-32.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Paola Pistidda, Laura Frogheri, Lina Oggiano, Luciana Guiso, Laura Manca, Fausto Dore, Bruno Masala, John G. Gilman & Maurizio Longinotti. (2006) Fetal hemoglobin expression in compound heterozygotes for −117 (G→A) A γ HPFH and β 0 39 nonsense thalassemia . American Journal of Hematology 49:4, pages 267-270.
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M. Longinotti, P. Pistidda, L. Oggiano, L. Guiso, L. Frogheri, F. Dore, S. Pardini, S. Bonfigli, E. Rimini, S. Angioni, P. Mulas & A. Inzaina. (2008) A 12‐year preventive program for β‐thalassemia in Northern Sardinia. Clinical Genetics 46:3, pages 238-243.
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LINA OGGIANO, ELENA RIMINI, LAURA FROGHERI, LUCIANA GUISO, PAOLA PISTIDDA & MAURIZIO LONGINOTTI. (2008) Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations. Clinical & Laboratory Haematology 14:4, pages 289-292.
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Bruno Masala & Laura Manca. (1990) High-performance liquid chromatography of globin chains in the identification of human globin gene abnormalities.. Biophysical Chemistry 37:1-3, pages 225-230.
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