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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