# Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing

**Authors:** Pål Marius Bjørnstad, Ragnhild Aaløkken, June Åsheim, Arvind Y. M. Sundaram, Caroline N. Felde, G. Henriette Østby, Marianne Dalland, Wenche Sjursen, Christian Carrizosa, Magnus D. Vigeland, Hanne S. Sorte, Ying Sheng, Sarah L. Ariansen, Eli Marie Grindedal, Gregor D. Gilfillan

PMC · DOI: 10.1038/s41431-023-01519-1 · 2024-01-04

## Full-text entities

- **Diseases:** Lynch syndrome (MESH:D003123)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11061170/full.md

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Source: https://tomesphere.com/paper/PMC11061170