Alhashmi, M., Gremida, A. M. E., Maharana, S. K., Antonaci, M., Kerr, A., Fu, S., . . . Yamamoto, K. Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation. Nature Publishing Group.
Chicago Style (17th ed.) CitationAlhashmi, Mohammad, et al. Skeletal Progenitor LRP1 Deficiency Causes Severe and Persistent Skeletal Defects with Wnt Pathway Dysregulation. Nature Publishing Group.
MLA (9th ed.) CitationAlhashmi, Mohammad, et al. Skeletal Progenitor LRP1 Deficiency Causes Severe and Persistent Skeletal Defects with Wnt Pathway Dysregulation. Nature Publishing Group.
Warning: These citations may not always be 100% accurate.