Stoffel, W., Jenke, B., Holz, B., Binczek, E., Günter, R. H., Knifka, J., . . . Niehoff, A. (2007). Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression. American Society for Investigative Pathology.
Citação norma ChicagoStoffel, Wilhelm, Britta Jenke, Barbara Holz, Erika Binczek, Robert Heinz Günter, Jutta Knifka, Jürgen Koebke, and Anja Niehoff. Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued By Col2A1-Driven Smpd3 Transgene Expression. American Society for Investigative Pathology, 2007.
ציטוט MLAStoffel, Wilhelm, et al. Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued By Col2A1-Driven Smpd3 Transgene Expression. American Society for Investigative Pathology, 2007.