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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 1
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Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family

Mehdi Haghi Department of Biology-Genetics, Science Faculty, Tabriz University, Tabriz, Iran
,
Abbas A. Hosseinpour Feizi Hematology-Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
,
Cornelis L. Harteveld Department of Clinical Genetics, Leiden University of Medical Center, Leiden, The Netherlands
,
Nasser Pouladi Department of Biology, Science Faculty, Azerbaijan University of Tarbiat Moallem, Tabriz, Iran
&
Mohammad A. Hosseinpour Feizi Department of Biology-Genetics, Science Faculty, Tabriz University, Tabriz, IranCorrespondence[email protected] [email protected]
Pages 75-80 | Received 03 Sep 2007, Accepted 15 Sep 2008, Published online: 07 Jul 2009

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