Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the A gamma-158 C > T mutation in gamma-globin gene transcription
dc.creator | Kollia, P. | en |
dc.creator | Kalamaras, A. | en |
dc.creator | Chassanidis, C. | en |
dc.creator | Samara, M. | en |
dc.creator | Vamvakopoulos, N. K. | en |
dc.creator | Radmilovic, M. | en |
dc.creator | Pavlovic, S. | en |
dc.creator | Papadakis, M. N. | en |
dc.creator | Patrinos, G. P. | en |
dc.date.accessioned | 2015-11-23T10:35:14Z | |
dc.date.available | 2015-11-23T10:35:14Z | |
dc.date.issued | 2008 | |
dc.identifier | 10.1016/j.bcmd.2008.05.009 | |
dc.identifier.issn | 1079-9796 | |
dc.identifier.uri | http://hdl.handle.net/11615/29534 | |
dc.source | Blood Cells Molecules and Diseases | en |
dc.source.uri | <Go to ISI>://WOS:000260150700007 | |
dc.subject | Hematology | en |
dc.title | Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the A gamma-158 C > T mutation in gamma-globin gene transcription | en |
dc.type | journalArticle | en |
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