Etiology of TP53 mutated complex karyotype acute myeloid leukemia
А. А. Феденко, H. Czapinska, Alwin Krämer, Friedrich Stölzel, Tilmann Bochtler, Matthias Bochtler
原始摘要（英文原文）· Original 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.