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Publication

Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome

Book Contribution - Book Abstract Conference Contribution

Book: EUROPEAN JOURNAL OF HUMAN GENETICS
Volume: 30
Pages: 40 - 41

Authors/publisher

  • Lore Pottie (Author)
  • Christin S. Adamo (Author)
  • Aude Beyens (Author)
  • Steffen Luetke (Author)
  • Piyanoot Tapaneeyaphan (Author)
  • Adelbert De Clercq (Author)
  • Phil Salmon (Author)
  • Rita De Rycke (Author)
  • Alper Gezdirici (Author)
  • Elif Yilmaz Gulec (Author)
  • Naz Khan (Author)
  • Jill E. Urquhart (Author)
  • William G. Newman (Author)
  • Kay Metcalfe (Author)
  • Stephanie Efthymiou (Author)
  • Reza Maroofian (Author)
  • Najwa Anwar (Author)
  • Shazia Maqbool (Author)
  • Fatima Rahman (Author)
  • Ikhlass Altweijri (Author)
  • Monerah Alsaleh (Author)
  • Sawsan Mohamed Abdullah (Author)
  • Mohammad Al-Owain (Author)
  • Mais Hashem (Author)
  • Henry Houlden (Author)
  • Fowzan S. Alkuraya (Author)
  • Patrick Sips (Author)
  • Gerhard Sengle (Author)
  • Bert Callewaert (Author)

Research units