Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

Abstract Loss-of-function germline variants of MLH1 cause Lynch syndrome. Here, we present the case of a 43-year-old male patient diagnosed with cecal and transverse colon adenocarcinomas. The characteristics of the case met the revised Bethesda guidelines, and the tumors demonstrated a high frequen...

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Bibliographic Details
Main Authors: Nobue Takaiso, Issei Imoto, Toshihiko Matsumoto, Akiyo Yoshimura
Format: Article
Language:English
Published: Nature Publishing Group 2024-09-01
Series:Human Genome Variation
Online Access:https://doi.org/10.1038/s41439-024-00294-9
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