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Publication

Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophyand hearing loss

Book Contribution - Book Abstract Conference Contribution

Book: EUROPEAN JOURNAL OF HUMAN GENETICS
Volume: 30
Pages: 45 - 45
Publication year:2022
Accessibility:Closed

Authors/publisher

  • Giulia Ascari (Author)
  • Nanna D. Rendtorff (Author)
  • Marieke De Bruyne (Author)
  • Julie De Zaeytijd (Author)
  • Michel Van Lint (Author)
  • Mattias Van Heetvelde (Author)
  • Gavin Arno (Author)
  • Julie Jacob (Author)
  • David Creytens (Author)
  • Jo Van Dorpe (Author)
  • Thalia Van Laethem (Author)
  • Toon Rosseel (Author)
  • Tim De Pooter (Author)
  • Peter De Rijk (Author)
  • Wouter De Coster (Author)
  • Björn Menten (Author)
  • Alfredo Dueñas Rey (Author)
  • Mojca Strazisar (Author)
  • Mette Bertelsen (Author)
  • Lisbeth Tranebjaerg (Author)
  • Elfride De Baere (Author)

Research units