%0 Journal Article
%T Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
%J -
%D 2019
%R https://doi.org/10.1016/j.ccell.2018.12.011
%X £¿ Biallelic germline NTHL1 mutations predispose to a multi-tumor syndrome £¿ Biallelic germline NTHL1 mutation carriers are at risk for breast cancer £¿ Tumors from NTHL1-deficient patients reveal a cross-cancer NTHL1-associated signature £¿ Mutational signature analyses can assist to identify germline DNA repair defect
%U https://www.cell.com/cancer-cell/fulltext/S1535-6108(18)30583-X