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Autor:
Asma Ounalli, Imen Moumni, Amal Mechaal, Aya Chakroun, Mbarka Barmat, Rim El Elj Rhim, Samia Menif, Ines Safra
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundGenetic variations in TP53 gene are known to be important in chronic lymphocytic leukemia (CLL) and may cause its inactivation which is associated with an aggressive form of the disease. Single nucleotide polymorphism (rs1042522:G>C) in TP5
Externí odkaz:
https://doaj.org/article/861ae5c3c4f14461a3a0488c10b6ac63
