DiStasio, A., Driver, A., Sund, K., Donlin, M., Muraleedharan, R. M., Pooya, S., . . . Stottmann, R. W. (2017). Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly. Hum Mol Genet.
Chicago ZitierstilDiStasio, Andrew, et al. "Copb2 Is Essential for Embryogenesis and Hypomorphic Mutations Cause Human Microcephaly." Hum Mol Genet 2017.
MLA ZitierstilDiStasio, Andrew, et al. "Copb2 Is Essential for Embryogenesis and Hypomorphic Mutations Cause Human Microcephaly." Hum Mol Genet 2017.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.