Cundy, T., Dray, M., Delahunt, J., Hald, J. D., Langdahl, B., Li, C., Szybowska, M., Mohammed, S., Duncan, E. L., McInerney‐Leo, A. M., Wheeler, P. G., Roschger, P., Klaushofer, K., Rai, J., Weis, M., Eyre, D., Schwarze, U., & Byers, P. H. (2018). mutations That Alter the Carboxy‐Terminal‐Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype. Journal of bone and mineral research, 33, 1260–1271. http://access.bl.uk/ark:/81055/vdc_100066531430.0x000049