DNA repair genes and chronic myeloid leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) gene polymorphisms
![Thumbnail](/xmlui/bitstream/handle/20.500.12511/6666/Ozdilli-Kursat-2021.pdf.jpg?sequence=4&isAllowed=y)
View/ Open
Access
info:eu-repo/semantics/openAccessAttribution-NonCommercial 4.0 Internationalhttps://creativecommons.org/licenses/by-nc/4.0/Date
2021Author
Özdilli, KürşatPehlivan, Mustafa
Serin, İstemi
Oğuz Savran, Fatma
Tomatır, Ayşe Gaye
Pehlivan, Sacide
Metadata
Show full item recordCitation
Özdilli, K., Pehlivan, M., Serin, İ., Oğuz Savran, F., Tomatır, A. G. ve Pehlivan, S. (2021). DNA repair genes and chronic myeloid leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) gene polymorphisms. Mediterranean Journal of Hematology and Infectious Diseases, 13. https://dx.doi.org/10.4084/MJHID.2021.020Abstract
To the editor. Chronic myeloid leukemia (CML), which is characterized by the overproduction of mature cells in the granulocytic series, is included in the group of chronic myeloproliferative neoplasms.1 It is the first disease ascertained as due to a specific chromosomal anomaly emerging from a reciprocal translocation between chromosomes 9 and 22. A chimeric gene denominated as the Philadelphia (Ph) chromosome is the product of the fusion of the Abelson oncogene (ABL) from chromosome 9q34 with the breakpoint cluster region (BCR) on chromosome 22q11.2, t (9;22)(q34;q11.2).