Etiology of TP53 mutated complex karyotype acute myeloid leukemia

TP53突变复杂核型急性髓系白血病的病因

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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.

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