MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years
Abstract
Lynch syndrome, is an autosomal dominantly inherited disease that predisposes individuals to a high risk of colorectal cancers, and some mismatch-repair genes have been identified as causative genes. The purpose of this study was to investigate the genomic rearrangement of the gene in a family with Lynch syndrome followed for more than 45 years.The family with Lynch syndrome is family N, who received colorectal cancer treatment for 45 years. The...
Paper Details
Title
MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years
Published Date
May 2, 2019
Journal
Volume
20
Issue
1
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