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The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1.

Ferdy K CayamiAlessandra MaugeriSanne TreurnietEva D SetijowatiBernd P TeunissenElisabeth M W EekhoffGerard PalsSultana M FaradzDimitra Micha
Published in: Molecular genetics & genomic medicine (2019)
We report a novel homozygous CREB3L1 mutation in a large Indonesian family; the homozygous affected members have survived to adulthood and they present a more severe phenotype than previously reported, expanding the clinical spectrum of OI for this gene.
Keyphrases
  • depressive symptoms
  • genome wide
  • early onset
  • dna methylation
  • genome wide identification
  • young adults
  • drug induced
  • bone regeneration