Zlatic, S. A., Vrailas-Mortimer, A., Gokhale, A., Carey, L. J., Scott, E., Burch, R., . . . Faundez, V. (2018). Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees. Cell Syst.
Citação norma ChicagoZlatic, Stephanie A., et al. "Rare Disease Mechanisms Identified By Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees." Cell Syst 2018.
Citação norma MLAZlatic, Stephanie A., et al. "Rare Disease Mechanisms Identified By Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees." Cell Syst 2018.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.