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A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing.
Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD. Bjørnstad PM, et al. Among authors: asheim j. Eur J Hum Genet. 2023 Nov 29. doi: 10.1038/s41431-023-01494-7. Online ahead of print. Eur J Hum Genet. 2023. PMID: 38030917
Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.
Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD. Bjørnstad PM, et al. Among authors: asheim j. Eur J Hum Genet. 2024 Jan 4. doi: 10.1038/s41431-023-01519-1. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38172175 No abstract available.