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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 5
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Original Article

The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT

Luke ForsterDepartment of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Center, Nedlands, Western Australia;School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western Australia
,
Rasha Mesbah ArdakaniDepartment of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Center, Nedlands, Western Australia
,
Talal QadahDepartment of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Center, Nedlands, Western Australia;School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western Australia;Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
,
Jill FinlaysonDepartment of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Center, Nedlands, Western Australia;School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western Australia
&
Reza GhassemifarDepartment of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Center, Nedlands, Western Australia;School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western AustraliaCorrespondence[email protected]
Pages 334-339 | Received 21 Jan 2015, Accepted 02 Apr 2015, Published online: 24 Jul 2015

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Wissem Abdaoui, Djamel Eddine Benouareth, Amel Djenouni, Celine Renoux, Fatiha Grifi, Adel Gouri, Fateh Athamnia, Manel Benalioua & Philippe Joly. (2019) Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15) . Hemoglobin 43:4-5, pages 223-228.
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Supachai Ekwattanakit, Suchada Riolueang & Vip Viprakasit. (2018) Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β0 thalassemia. Hematology 23:2, pages 117-121.
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