MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
Abstract
<b><i>Introduction:</i></b> Deleterious heterozygous mutation of the MLH1 gene is an important cause of Lynch syndrome (LS), an autosomal dominant cancer caused by functional defects in the DNA mismatch repair (MMR) complex. <b><i>Case Report:</i></b> The proband was a 35-year-old patient with confirmed colorectal cancer (CRC). Immunohistochemical (IHC) staining revealed the absence of MLH1 and...
Paper Details
Title
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
Published Date
Jan 1, 2021
Volume
44
Issue
7-8
Pages
414 - 421
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