Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype
A. Rübben, R. U. Wahl, T. Eggermann, E. Dahl, N. Ortiz-Brüchle, C. Cacchi
This paper identifies somatic mutations in CTNNB1 in multiple pilomatricomas and a pilomatrical carcinoma from a DM1 patient, suggesting a tissue- and gene-specific hypermutation phenotype.
bioRxiv · Nov 15, 2019Cancer Biology