Alhashmi, M, Gremida, AME, Maharana, SK, Antonaci, M, Kerr, A, Fu, S, Lunn, S, Turner, DA, Al-Maslamani, NA, Liu, K, Meschis, MM, Sutherland, H, Wilson, P, Clegg, P, Wheeler, GN, van 't Hof, RJ, Bou-Gharios, G and Yamamoto, K (2025) Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation. Bone Research, 13. ISSN 2095-4700