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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 3
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Original Article

A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (GAG→TAG) in a Tunisian Family

Hajer Siala Laboratoire de Biochimie, Clinique‐Hôpital d'Enfants, Tunis, 1007, Tunisia
,
Slaheddine Fattoum Laboratoire de Biochimie, Clinique‐Hôpital d'Enfants, Tunis, 1007, Tunisia
,
Taieb Messaoud Laboratoire de Biochimie, Clinique‐Hôpital d'Enfants, Tunis, 1007, Tunisia
,
Fadiq Ouali Laboratoire de Biochimie, Clinique‐Hôpital d'Enfants, Tunis, 1007, Tunisia
,
Nathalie Gerard INSERM UMR458, Hôpital Robert Debré, 48 Bd Serurier, 75019, Paris, France
&
Rajagopal Krishnamoorthy INSERM UMR458, Hôpital Robert Debré, 48 Bd Serurier, 75019, Paris, France
Pages 249-254 | Received 10 Nov 2003, Accepted 23 Dec 2003, Published online: 24 Aug 2009

Citations (9)

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Read on this site (4)

Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia. Hemoglobin 39:6, pages 398-402.
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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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Barry Eng, Lynda Walker & John S. Waye. (2009) α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG). Hemoglobin 33:1, pages 72-74.
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Hajer Siala, Faida Ouali, Taieb Messaoud, Rachida Sfar & Slaheddine Fattoum. (2005) 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. Hemoglobin 29:4, pages 263-268.
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Articles from other publishers (5)

Paloma Ropero, Ana Villegas, Jorge M. Nieto, Fernando A. González & Rafael Martínez. (2019) Novel nonsense mutation in the α1-globin gene [HBA1:C.49A>T] is responsible for non-deletion α-thalassemia. Clinical Biochemistry 63, pages 139-142.
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Giovanna Cardiero, Clelia Scarano, Gennaro Musollino, Francesca Di Noce, Romeo Prezioso, Sabrina Dembech, Gaetana La Porta, Mercedes Caldora, Maria Grazia Bisconte, Rosario Colella Bisogno & Giuseppina Lacerra. (2017) Role of nonsense-mediated decay and nonsense-associated altered splicing in the mRNA pattern of two new α-thalassemia mutants. The International Journal of Biochemistry & Cell Biology 91, pages 212-222.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
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.
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