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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 4
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Short Communication

Codon 14 (+T) (HBB: c.44_45insT): a Rare β-Thalassemia Mutation Reported Only in Azerbaijan

Gunay AliyevaDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-1751-3684
ORCID Icon,
Chingiz AsadovDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan;
,
Tahira MammadovaDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan;
,
Shirkhan MusayevNS Genetics, Baku, Azerbaijan
,
Eldar AbdulalimovDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan;
,
Surmaya GafarovaDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan;
&
Yegana GuliyevaDepartment of Haemopoietic Pathologies, Institute of Hematology and Blood Transfusion, Baku, Azerbaijan;
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Pages 276-277 | Received 10 Aug 2018, Accepted 18 Sep 2018, Published online: 13 Nov 2018

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Bayram Bayramov, Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Nigar Karimova, Khagani Eynullazadeh, Surmaya Gafarova, Seymur Akbarov, Sabina Farhadova, Zumrud Safarzadeh & Mehraj Abbasov. (2019) A Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan. Hemoglobin 43:4-5, pages 280-282.
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Articles from other publishers (1)

Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Surmaya Gafarova, Yegana Guliyeva & Eldar Abdulalimov. (2019) Molecular and geographical heterogeneity of hemoglobinopathy mutations in Azerbaijanian populations. Annals of Human Genetics 84:3, pages 249-258.
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