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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
| Naziv: | 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 | Autori: | Kollia, Panagoula; Kalamaras, Angelos; Chassanidis, Christos; Samara, Maria; Vamvakopoulos, Nikolaos K.; Ugrin, Milena |
Godina: | 2008 | Publikacija: | Blood Cells Molecules and Diseases | ISSN: | 1079-9796 Blood Cells Molecules and Diseases Pretraži identifikator |
Izdavač: | Academic Press Inc Elsevier Science, San Diego | Tip rezultata: | Informativni prilog | Kolacija: | 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-kategorija: | 22M22 - Međunarodni časopis kategorije M22 |
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