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Identification of a novel intergenic EPCAM-MSH2 deletion causing EPCAM-associated Lynch syndrome by long-read nanopore sequencing

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Clinical researchRead the full text
  • Published on:
  • Source: Journal of Medical Genetics
Authors: Luiza Steffens Reinhardt, Alexander Coster, Sean M Burnard, Caitlin S Romanis, Andrew Ziolkowski, Gordana Pecenpetelovska, Andrea Mathe, Amelia Hedley, Vicki E Maltby, Jeannette Lechner-Scott, Katie Ashton, Kelly A Avery-Kiejda, Rodney J Scott

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