Research Alert

Newswise — Sebert, Gachet et al. analyzed longitudinal data from patients with Fanconi anemia, a rare inherited DNA-repair disease. They provided genomic and functional insights into MDM4-driven p53 response modulation yielding clonal hematopoiesis and preceding transformation to myeloid leukemia in the background of chromosomal instability and HSC attrition.

Journal Link: Publisher Website Journal Link: Download PDF

MEDIA CONTACT
Register for reporter access to contact details
CITATIONS

DOI link; Publisher Website; Download PDF