Carla Caffarelli, Stefano Gonnelli, Maria Dea Tomai Pitinca, Silvia Camarri, Antonella Al Refaie, Joussef Hayek, & Ranuccio Nuti. (2020). Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome. BMC.
Chicago Style (17th ed.) CitationCarla Caffarelli, Stefano Gonnelli, Maria Dea Tomai Pitinca, Silvia Camarri, Antonella Al Refaie, Joussef Hayek, and Ranuccio Nuti. Methyl-CpG-binding Protein 2 (MECP2) Mutation Type Is Associated with Bone Disease Severity in Rett Syndrome. BMC, 2020.
MLA (9th ed.) CitationCarla Caffarelli, et al. Methyl-CpG-binding Protein 2 (MECP2) Mutation Type Is Associated with Bone Disease Severity in Rett Syndrome. BMC, 2020.
Warning: These citations may not always be 100% accurate.