De novo and inherited pathogenic variants in collagen-related osteogenesis imperfecta.
Lidiia ZhytnikKatre MaasaluBinh Ho DuyAndrey PashenkoSergey KhmyzovEne ReimannEle PransSulev KõksAare MärtsonPublished in: Molecular genetics & genomic medicine (2019)
In summary, there were significant differences between the phenotypes and genotypes of subjects with de novo and inherited OI. These findings may promote the further understanding of OI etiology, and assist with diagnostics procedures, as well as with family planning.