Cita APA

Meuwissen, M. E., Schot, R., Buta, S., Oudesluijs, G., Tinschert, S., Speer, S. D., . . . Mancini, G. M. (2016). Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome. J Exp Med.

Chicago Style Citation

Meuwissen, Marije E.C., et al. "Human USP18 Deficiency Underlies Type 1 Interferonopathy Leading to Severe Pseudo-TORCH Syndrome." J Exp Med 2016.

Cita MLA

Meuwissen, Marije E.C., et al. "Human USP18 Deficiency Underlies Type 1 Interferonopathy Leading to Severe Pseudo-TORCH Syndrome." J Exp Med 2016.