Publication | Open Access

Value of MLH1 and MSH2 Mutations in the Appearance of Muir–Torre Syndrome Phenotype in HNPCC Patients Presenting Sebaceous Gland Tumors or Keratoacanthomas

Msh2 MutationsTumor BiologyGenetic DisorderHnpcc PatientsPathologyMuir–torre Syndrome PhenotypeDermatologyCancer GeneticsMedicineCancer ResearchMolecular Oncology