D, S., R, T. G., V, C., G, G., R, C., V, C., . . . S, M. (2020). Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1866, 165793. https://doi.org/10.1016/j.bbadis.2020.165793
Chicago Style (17th ed.) CitationD, Sbardella, et al. "Defective Proteasome Biogenesis into Skin Fibroblasts Isolated from Rett Syndrome Subjects with MeCP2 Non-sense Mutations." Biochimica Et Biophysica Acta (BBA) - Molecular Basis of Disease 1866 (2020): 165793. https://doi.org/10.1016/j.bbadis.2020.165793.
MLA (9th ed.) CitationD, Sbardella, et al. "Defective Proteasome Biogenesis into Skin Fibroblasts Isolated from Rett Syndrome Subjects with MeCP2 Non-sense Mutations." Biochimica Et Biophysica Acta (BBA) - Molecular Basis of Disease, vol. 1866, 2020, p. 165793, https://doi.org/10.1016/j.bbadis.2020.165793.