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

Homozygosity for the AATAAA > AATA– – Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report

Samaneh FarashiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran;Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran
,
Negin F. GarousKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran
,
Mehri AshkiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran
,
Shadi VakiliKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran
,
Fatemeh ZeinaliKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran
,
Hashem ImanianKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran
,
Azita AzarkeivanKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran;Iranian Blood Transfusion Organization, High Institute for Transfusion Research Center, Tehran, Iran
,
Piero C. GiordanoDepartment of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The NetherlandsCorrespondence[email protected]
&
Hossein NajmabadiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran;Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran
 show all
Pages 355-358 | Received 24 Jan 2015, Accepted 25 Feb 2015, Published online: 21 Jul 2015

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Read on this site (2)

Qiang Zhang, Xin Fan, Mingli Xu, Yijia Zhang, Huiling Xu, Xiaojun Wen & Wanjun Zhou. (2017) Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα. Hemoglobin 41:3, pages 189-192.
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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