Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation
| Title: | Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation |
|---|---|
| Authors: | Alhashmi, MohammadAff1, Aff3, Aff4; Gremida, Abdulrahman M. E.Aff1; Maharana, Santosh K.Aff2; Antonaci, MarcoAff2; Kerr, AmyAff2; Fu, ShijianAff1; Lunn, SharnaAff1; Turner, David A.Aff1; Al-Maslamani, Noor A.Aff1; Liu, KeAff1; Meschis, Maria M.Aff1; Sutherland, HazelAff1; Wilson, PeterAff1; Clegg, PeterAff1; Wheeler, Grant N.Aff2; van ‘t Hof, Robert J.Aff1, Aff5; Bou-Gharios, GeorgeAff1; Yamamoto, KazuhiroAff1, IDs4141302400393x_cor1 |
| Source: | Bone Research. 13(1) |
| Database: | Springer Nature Journals |