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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2024 Jan 4;32(5):601–602. doi: 10.1038/s41431-023-01519-1

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

Pål Marius Bjørnstad 1,#, Ragnhild Aaløkken 1,#, June Åsheim 1,#, Arvind Y M Sundaram 1,#, Caroline N Felde 1, G Henriette Østby 1, Marianne Dalland 1, Wenche Sjursen 2, Christian Carrizosa 1, Magnus D Vigeland 1,3, Hanne S Sorte 1, Ying Sheng 1, Sarah L Ariansen 1, Eli Marie Grindedal 1,#, Gregor D Gilfillan 1,✉,#
PMCID: PMC11061170  PMID: 38172175

Correction to: European Journal of Human Genetics 10.1038/s41431-023-01494-7, published online 29 November 2023

In this article, the wrong figure appeared as Fig. 3B due to typesetting mistake.; the Fig. 3 should have appeared as shown below.

graphic file with name 41431_2023_1519_Figa_HTML.jpg

The original article has been corrected.


Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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