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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 4
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Original Article

First Description in Tunisia of a Point Mutation at Codon 119 (CCT→TCT) in the α1-Globin Gene: Hb Groene Hart in Association with the − α3.7 Deletion

Hajer Siala Laboratoire de Biochimie Clinique, Hôpital d'Enfants, Tunis, Tunisie
,
Faida Ouali Laboratoire de Biochimie Clinique, Hôpital d'Enfants, Tunis, Tunisie
,
Taieb Messaoud Laboratoire de Biochimie Clinique, Hôpital d'Enfants, Tunis, Tunisie
,
Rachida Sfar Maternité, Hôpital Charles Nicole, Tunis, Tunisie
&
Slaheddine Fattoum Laboratoire de Biochimie Clinique, Hôpital d'Enfants, Tunis, TunisieCorrespondence[email protected]
, M.D.
Pages 263-268 | Received 04 Apr 2005, Accepted 02 May 2005, Published online: 07 Jul 2009

Citations (14)

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Philippe Joly, Philippe Lacan, Caroline Garcia & Alain Francina. (2014) Description of the Phenotypes of 63 Heterozygous, Homozygous and Compound Heterozygous Patients Carrying the Hb Groene Hart [α119(H2)Pro→Ser; HBA1: c.358C>T] Variant. Hemoglobin 38:1, pages 64-66.
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Philippe Joly, Philippe Lacan, Caroline Garcia & Alain Francina. (2013) Two Complex Associations of an HBD Mutation and a Rare α Hemoglobinopathy. Hemoglobin 37:5, pages 486-491.
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Stephen O. Brennan, Tim Chan & Jaine Duncan. (2012) Novel α2 Gene Deletion (c.349_359 del GAGTTCACCCC) Identified in Association with the –α3.7 Deletion. Hemoglobin 36:1, pages 93-97.
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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Piero C. Giordano, Sonja Zweegman, Nicole Akkermans, Sandra G.J. Arkesteijn, Peter van Delft, Florens G.A. Versteegh, Henri Wajcman & Cornelis L. Harteveld. (2007) The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant. Hemoglobin 31:2, pages 179-182.
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Articles from other publishers (8)

A. Zorai, I. Moumni, I. Mosbahi, K. Douzi, D. Chaouachi, F. Guemira & S. Abbes. (2015) Rare hemoglobin variants in Tunisian population. International Journal of Laboratory Hematology 37:2, pages 148-154.
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Félix de la Fuente-Gonzalo, Paloma Ropero, Jorge Martínez-Nieto, Ana Villegas, Fernando A. González & Joaquín Díaz-Mediavilla. (2015) Asociación de la hemoglobina Groene Hart con la hemoglobina J-París-I: primer caso en España. Medicina Clínica 144:5, pages 212-215.
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Félix de la Fuente-Gonzalo, Paloma Ropero, Jorge Martínez-Nieto, Ana Villegas, Fernando A. González & Joaquín Díaz-Mediavilla. (2015) Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: First case in Spain. Medicina Clínica (English Edition) 144:5, pages 212-215.
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Lilia Romdhane & Sonia Abdelhak. (2010) Genetic diseases in the Tunisian population. American Journal of Medical Genetics Part A 155:1, pages 238-267.
Crossref
Xiang YuTodd L. MollanAndrew Butler, Andrew J. Gow, John S. OlsonMitchell J. Weiss. (2009) Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein. Blood 113:23, pages 5961-5969.
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H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
Crossref
Isabelle Zanella-Cleon, Michel Becchi, Philippe Lacan, Piero C Giordano, Henri Wajcman & Alain Francina. (2008) Detection of a Thalassemic α-Chain Variant (Hemoglobin Groene Hart) by Reversed-Phase Liquid Chromatography. Clinical Chemistry 54:6, pages 1053-1059.
Crossref
Corinne Vasseur-Godbillon, Michael C. Marden, Piero Giordano, Henri Wajcman & Véronique Baudin-Creuza. (2006) Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells, Molecules, and Diseases 37:3, pages 173-179.
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