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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Original Article

Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene

Samaneh FarashiGenetics Research Centre, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran ;Department of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Shadi VakiliDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Negin F. GarousDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Mehri AshkiDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Fatemeh Forouzesh PourDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Fatemeh ZeinaliDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Fariba RadDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Hashem ImanianDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran
,
Azita AzarkeivanDepartment of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran ;Iranian Blood Transfusion Organization, High Institute for Transfusion Research Centre, Tehran, Iran
&
Hossein NajmabadiGenetics Research Centre, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran ;Department of Molecular Genetics, Kariminejad-Najmabadi Pathology & Genetics Centre, Tehran, Iran Correspondence[email protected]
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Pages 38-43 | Received 27 Apr 2015, Accepted 08 Aug 2015, Published online: 04 Nov 2015

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Read on this site (1)

Azita Azarkeivan, Nader Cohan, Hamid Reza Niazkar, Arsalan Azizi & Fariba Rad. (2020) Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients . Hemoglobin 44:2, pages 109-112.
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Articles from other publishers (1)

Samaneh Farashi & Cornelis L. Harteveld. (2018) Molecular basis of α-thalassemia. Blood Cells, Molecules, and Diseases 70, pages 43-53.
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