Skip to main navigation Skip to search Skip to main content

Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

  • Marc Pauper
  • , Erdi Kucuk
  • , Aaron M Wenger
  • , Shreyasee Chakraborty
  • , Primo Baybayan
  • , Michael Kwint
  • , Bart van der Sanden
  • , Marcel R Nelen
  • , Ronny Derks
  • , Han G Brunner
  • , Alexander Hoischen
  • , Lisenka E L M Vissers
  • , Christian Gilissen*
  • *Corresponding author for this work

Research output: Contribution to journalErratum / corrigendumAcademic

Abstract

The authors inadvertently included tracked changes in their Supplemental Material file in error. These have been now been removed.

Original languageEnglish
Pages (from-to)720-720
Number of pages1
JournalEuropean Journal of Human Genetics
Volume29
Issue number4
DOIs
Publication statusPublished - Apr 2021

Fingerprint

Dive into the research topics of 'Correction: Long-read trio sequencing of individuals with unsolved intellectual disability'. Together they form a unique fingerprint.
  • Long-read trio sequencing of individuals with unsolved intellectual disability

    Pauper, M., Kucuk, E., Wenger, A. M., Chakraborty, S., Baybayan, P., Kwint, M., van der Sanden, B., Nelen, M. R., Derks, R., Brunner, H. G., Hoischen, A., Vissers, L. E. L. M. & Gilissen, C., Apr 2021, In: European Journal of Human Genetics. 29, 4, p. 637-648 12 p.

    Research output: Contribution to journalArticleAcademicpeer-review

    Open Access

Cite this