Etiology of TP53 mutated complex karyotype acute myeloid leukemia.
SCHEMATIC VIEW OF THE DEVELOPMENT OF CK-AML DRIVEN BY THE TP53 ABSENCE.: The occurrence of the first, often dominant negative TP53 mutation is quickly followed by the loss of the second TP53 allele an
APA
Fedenko A, Czapinska H, et al. (2026). Etiology of TP53 mutated complex karyotype acute myeloid leukemia.. Leukemia, 40(2), 444-448. https://doi.org/10.1038/s41375-025-02835-9
MLA
Fedenko A, et al.. "Etiology of TP53 mutated complex karyotype acute myeloid leukemia.." Leukemia, vol. 40, no. 2, 2026, pp. 444-448.
PMID
41419603
Abstract
SCHEMATIC VIEW OF THE DEVELOPMENT OF CK-AML DRIVEN BY THE TP53 ABSENCE.: The occurrence of the first, often dominant negative TP53 mutation is quickly followed by the loss of the second TP53 allele and numerous further chromosomal aberrations.
MeSH Terms
Humans; Leukemia, Myeloid, Acute; Mutation; Tumor Suppressor Protein p53; Chromosome Aberrations; Karyotype; Karyotyping