Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-014-0343-y.pdf
Reference16 articles.
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3. Akhavan-Niaki H, Derakhshandeh-Peykar P, Banihashemi A et al (2011) A comprehensive molecular characterization of β thalassemia in a highly heterogeneous population. Blood Cells Mol Dis 47(1):29–32
4. Derakhshandeh-Peykar P, Akhavan-Niaki H, Tamaddoni A et al (2007) Distribution of β-thalassemia mutations in the northern provinces of Iran. Hemoglobin 31(3):351–356
5. Najmabadi H, Karimi-Nejad R, Sahebjam S et al (2001) The beta-thalassemia mutation spectrum in the Iranian population. Hemoglobin 25(3):285–296
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia;BMC Pediatrics;2019-02-18
2. Identification of a Neonate with Thalassemia Intermedia Despite Premarital Screening Program in Mazandaran Province (Co-inheritance of Hb Knossos and IVS II-1 G> A Mutations);Research in Molecular Medicine;2017-05-01
3. Identification of a Rareβ0-Thalassemia Mutation, Codon 54 (–T) (HBB: c.165delT) in an Iranian Family;Hemoglobin;2015-08-19
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