(1897801), N. A., (11704868), S. W., (496764), L. R., (18527778), R. J. v. H., (311778), S. H. R., & (18508167), O. M. A. (2021). Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.
Chicago Style (17th ed.) Citation(1897801), Nerea Alonso, Sachin Wani (11704868), Lorraine Rose (496764), Rob J. van't Hof (18527778), Stuart H. Ralston (311778), and Omar M.E. Albagha (18508167). Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice. 2021.
MLA (9th ed.) Citation(1897801), Nerea Alonso, et al. Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice. 2021.