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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 4
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Original Article

Thalassemia Intermedia Due to a Novel Mutation in the Second Intervening Sequence of the β-Globin Gene

Imane Agouti Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
,
Mohcine Bennani Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
,
Abouyoub Ahmed Centre Régional de Transfusion Sanguine de Rabat, Rabat, Maroc
,
Amina Barakat Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
,
Khattab Mohamed Service d'Hémato-Oncologie Pédiatrique, Hôpital d'Enfant, Rabat, Maroc
&
Catherine Badens Laboratoire de Génétique Moléculaire, Hôpital d'Enfant de la Timone, Marseille, FranceCorrespondence[email protected]
Pages 433-438 | Received 04 Apr 2007, Accepted 12 Jun 2007, Published online: 07 Jul 2009

Citations (4)

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Runa M. Grimholt, Cornelis L. Harteveld, Sandra G. J. Arkesteijn, Bente Fjeld & Olav Klingenberg. (2018) Characterization of Two Deep Intronic Variants on the β-Globin Gene with Inconsistent Interpretations of Clinical Significance. Hemoglobin 42:2, pages 126-128.
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Imane Agouti, Mohcine Bennani, Nicolas Levy, Piero Giordano & Catherine Badens. (2009) The Rare Codon 24 (T>A) (β+) Mutation in Association with the Common Codon 39 (C> T) (β0) Mutation Causes Transfusion-Dependent β-Thalassemia in a Moroccan Patient. Hemoglobin 33:2, pages 150-154.
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Articles from other publishers (2)

Petros Patsali, Claudio Mussolino, Petros Ladas, Argyro Floga, Annita Kolnagou, Soteroula Christou, Maria Sitarou, Michael N. Antoniou, Toni Cathomen, Carsten Werner Lederer & Marina Kleanthous. (2019) The Scope for Thalassemia Gene Therapy by Disruption of Aberrant Regulatory Elements. Journal of Clinical Medicine 8:11, pages 1959.
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Imane AgoutiCatherine BadensAhmed AbouyoubNicolas LevyMohcine Bennani. (2008) Molecular Basis of β-Thalassemia in Morocco: Possible Origins of the Molecular Heterogeneity. Genetic Testing 12:4, pages 563-568.
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