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4. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

6. USP7 inhibition alters homologous recombination repair and targets CLL cells independently of ATM/p53 functional status

7. Microarray analysis reveals that TP53- and ATM-mutant B-CLLs share a defect in activating proapoptotic responses after DNA damage but are distinguished by major differences in activating prosurvival responses

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