HIGHLIGHTS
- who: Kefeng Shen from the Center, United States Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of have published the Article: Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report, in the Journal: (JOURNAL) of 20/08/2020
SUMMARY
The Fanconi anemia (FA) pathway (also known as the FABRCA pathway) is involved in the repair of DNA lesions by homologous recombination, which plays a vital role in the maintenance of genomic stability. To date, researchers have already identified germline . . .
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