SavedAdd your journal

Journals / Turkish Journal of Hematology / 2011 / Cilt: 28 - Sayı: 4

Double heterozygosity of the thalassemic mutations term. Cd +6 C→G and IVS-I-110 in a Greek woman: A case presentation

Yunan bir kadında çift heterozigozit talasemik mutasyonlar terimi Cd +6 C → G ve IVS-I-110: Bir olgu sunumu

Stamatia THEODORIDOU
Vasilios PERIFANIS
Stella KOTSIOPOULOU
Olga KARAKASIDOU
Vasiliki ALETRA
Michael ALEMAYEHOU
Pages
341–342
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
🔖

Cite This Article

THEODORIDOU, S., PERIFANIS, V., KOTSIOPOULOU, S., KARAKASIDOU, O., ALETRA, V., ALEMAYEHOU, M. (2022). Double heterozygosity of the thalassemic mutations term. Cd +6 C→G and IVS-I-110 in a Greek woman: A case presentation. Turkish Journal of Hematology, Cilt: 28 - Sayı: 4, 341–342. https://ajindex.com/articles/606998

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (2)

  1. Jankovic L, Dimovski AJ, Kollia P, Karageorga M, Loukopoulos D, Huisman YH. A C----G mutation at nt position 6 3’ to the termination codon may be the cause of a silent beta-thalassemia. Int J Hematol 1991;54:289-93.
  2. Maragoudaki E, Vrettou C, Kanavakis E, Traeger- Synodinos J, Metaxoton-Mavrommati A, Kattamis C. Molecular, haematological and clinical studies of a silent β-gene C-G mutation at 6bp 3’ to the termination codon (+1480 C-G) in twelve Greek families. Br J Haematol 1998;103:45-51. [CrossRef] Boussiou M, Karababa Ph, Sinopoulou K, Tsaftaridis P Plata E, Loutradi-Anagnostou A. The molecular hetero- geneity of beta-thalassemia in Greece. Blood Cells Mol Dis 2008;40:317-9. [CrossRef]