https://pubmed.ncbi.nlm.nih.gov/21227399/
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases
Lynch syndrome is an autosomal dominant cancer predisposition syndrome characterized by loss of function of DNA mismatch repair enzyme MLH1, MSH2, MSH6, or...
lynch syndromefrequencydeletionsepcam