Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ - 158 C > T mutation in γ-globin gene transcription

2008-11-01

Blood Cells, Molecules and Diseases , Volume 41 - Issue 3 p. 263- 264

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Persistent URL	doi.org/10.1016/j.bcmd.2008.05.009, hdl.handle.net/1765/30180
Journal	Blood Cells, Molecules and Diseases
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Kollia, P., Kalamaras, A., Chassanidis, C., Samara, M., Vamvakopoulos, N., Radmilovic, M., … Patrinos, G. (2008). Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ - 158 C > T mutation in γ-globin gene transcription. Blood Cells, Molecules and Diseases, 41(3), 263–264. doi:10.1016/j.bcmd.2008.05.009

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