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

Eur J Hum Genet. 2024 May;32(5):601-602. doi: 10.1038/s41431-023-01519-1.

Authors

Pål Marius Bjørnstad^#¹, Ragnhild Aaløkken^#¹, June Åsheim^#¹, Arvind Y M Sundaram^#¹, Caroline N Felde¹, G Henriette Østby¹, Marianne Dalland¹, Wenche Sjursen², Christian Carrizosa¹, Magnus D Vigeland^{1

3}, Hanne S Sorte¹, Ying Sheng¹, Sarah L Ariansen¹, Eli Marie Grindedal^#¹, Gregor D Gilfillan^#⁴

Affiliations

¹ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
² Department of Clinical & Molecular Medicine, NTNU and Department of Medical Genetics, St Olavs Hospital, Trondheim, Norway.
³ Department of Forensic Sciences, Oslo University Hospital, 0372, Oslo, Norway.
⁴ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway. gregorg@medisin.uio.no.

^# Contributed equally.

No abstract available

Publication types

Published Erratum