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

First observation of hemoglobin Crete [Beta129(H7) Ala>Pro] in the Turkish population

Çiğdem ARSLAN
Selda KAHRAMAN
Hayri ÖZSAN
Nejat AKAR
Sayfa
346–347
DOI
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Bu Makaleye Atıf Yap

ARSLAN, Ç., KAHRAMAN, S., ÖZSAN, H., AKAR, N. (2011). First observation of hemoglobin Crete [Beta129(H7) Ala>Pro] in the Turkish population. Turkish Journal of Hematology, Cilt: 28 - Sayı: 4, 346–347. https://ajindex.com/articles/413166

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Kaynakça (5)

  1. Huismann THJ, Carver MFH, Efremov GDA. Syllabus of hemoglobin variants. The Sickle Cell Anemia Foundation. 2nd ed. GA, USA: Augusta, 1998.
  2. Maniatis A, Bousios T, Nagel RL, Balazs T, Ueda Y, Bookchin RM, Maniatis GM. Hemoglobin Crete (beta 129 ala leads to pro): a new high-affinity variant inter- acting with beta o -and delta beta o -thalassemia. Blood 1979;54:54-63.
  3. Christopoulou G, Tserga A, Patrinos GP Papadakis MN. Molecular characterization and diagnosis of Hb Crete [beta129(H7)Ala-->Pro]. Hemoglobin 2004;28:339-42. [CrossRef] Papassotiriou I, Traeger-Synodinos J, Marden MC, Kister J, Liapi D, Prome D, Stamoulakatou A, Wajcman H, Kanavakis E. The homozygous state for Hb Crete [beta129 (H7) Ala-->Pro] is associated with a complex phenotype including erythrocytosis and functional anemia. Blood Cells Mol Dis 2005;34:229-34. [CrossRef] Altay C. Abnormal Hemoglobins in Turkey. Turk J Haematol 2002;19:63-74.
  4. Akar E, Akar N. A review of abnormal hemoglobins in Turkey. Turk J Hematol 2007:24;2-3.
  5. Oner R, Oner C, Birben E, Sözen M, Gümrük F, Gürgey A, Altay C. beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 rela- tive to the beta-globin cap site. Br J Haematol 2001;115:90-4. [CrossRef]