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

First report from Turkey of a rare frameshift mutation [codons 9/10 (+T)] in the beta-globin gene

Sayfa
343–345
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
🔖

Bu Makaleye Atıf Yap

GÜNEŞAÇAR, R., ÇELİK, M. (2011). First report from Turkey of a rare frameshift mutation [codons 9/10 (+T)] in the beta-globin gene. Turkish Journal of Hematology, Cilt: 28 - Sayı: 4, 343–345. https://ajindex.com/articles/412892

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (2)

  1. Altay C, Basak AN. Molecular basis and prenatal diag- nosis of hemoglobinopathies in Turkey. Int J Pediatr Hematol Oncol 1995;2:283-90.
  2. Hardison RC, Chui DHK, Giardine B, Riemer C, Patrinos GP Anagnou N, Miller W, Wajcman H. HbVar: a relation database of human hemoglobin variants and thalas- semia mutations at the globin gene server. Hum Mutat 2002;19:225-33. [CrossRef] Patrinos GP Giardine B, Riemer C, Miller W, Chui DHK, Anagnou DP Wajcman H, Hardison RC. Improvement in HbVar human hemoglobin variants and thalassemia mutations for population and sequence variation stud- ies. Nucleic Acids Res 2004;32:537-41. [CrossRef] Cavdar AO, Arcasoy A. The incidence of ß-thalassemia and abnormal hemoglobins in Turkey. Acta Haematol 1971;45:312-8. [CrossRef] Basak AN. The molecular pathology of B-thalassemia in Turkey: The Bogazici University experience. Hemoglobin 2007;31:233-41. [CrossRef] Waye JS, Eng B, Oliveri NF, Chui DH. Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosis. Prenatal Diag 1994;14:929-32. [CrossRef] Rahimi Z, Muniz A, Parsian A. Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Mol Biol Rep 2010;37:149-50. [CrossRef] Aulehla-Scholz C, Basaran S, Agaoglu L, Arcasoy A, Holzgreve W, Miny P, Ridolfi F, Horst J. Molecular basis of beta-thalassemia in Turkey: detection of rare mutations by direct sequencing. Hum Genet 1990;84:195-7. [CrossRef]