Presentation of two new mutations in the 3′untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-021-04509-9.pdf
Reference31 articles.
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2. Pengon J, Svasti S, Kamchonwongpaisan S, Vattanaviboon P (2018) Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia. Hematol Oncol Stem Cell Ther 11(1):18–24
3. Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH (2001) The beta-thalassemia mutation spectrum in the Iranian population. Hemoglobin 25:285–296
4. Canatan D, Kose MR, Ustundag M, Haznedaroglu D, Ozbas S (2006) Hemoglobinopathy control program in Turkey. Public Health Genomics 9(2):124–126
5. Başak AN (2007) The molecular pathology of β-thalassemia in Turkey: the Boğaziçi University experience. Hemoglobin 31(2):233–241
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