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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 gt T mutation in gamma-globin gene transcription
| 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 gt T mutation in gamma-globin gene transcription | Authors: | Kollia, Panagoula; Kalamaras, Angelos; Chassanidis, Christos; Samara, Maria; Vamvakopoulos, Nikolaos K.; Ugrin, Milena   ; Pavlović, Sonja ; Papadakis, Manoussos N.; Patrinos, George P. |
Issue Date: | 2008 | Publication: | Blood Cells Molecules and Diseases | ISSN: | 1079-9796 Blood Cells Molecules and Diseases Search Idenfier |
Publisher: | Academic Press Inc Elsevier Science, San Diego | Type: | Contribution to periodical | Collation: | vol. 41 br. 3 str. 263-264 | DOI: | 10.1016/j.bcmd.2008.05.009 | WoS-ID: | 000260150700007 | Scopus-ID: | 2-s2.0-54849129300 | PMID: | 18718799 | URI: | https://imagine.imgge.bg.ac.rs/handle/123456789/321 https://enauka.gov.rs/handle/123456789/571494 |
M-category: | 22M22 |
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