Cita APA

Skrabl-Baumgartner, A., Plecko, B., Schmidt, W. M., König, N., Hershfield, M., Gruber-Sedlmayr, U., & Lee-Kirsch, M. A. (2017). Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation. Pediatr Rheumatol Online J.

Chicago Style Citation

Skrabl-Baumgartner, Andrea, Barbara Plecko, Wolfgang M. Schmidt, Nadja König, Michael Hershfield, Ursula Gruber-Sedlmayr, i Min Ae Lee-Kirsch. "Autoimmune Phenotype With Type I Interferon Signature in Two Brothers With ADA2 Deficiency Carrying a Novel CECR1 Mutation." Pediatr Rheumatol Online J 2017.

Cita MLA

Skrabl-Baumgartner, Andrea, et al. "Autoimmune Phenotype With Type I Interferon Signature in Two Brothers With ADA2 Deficiency Carrying a Novel CECR1 Mutation." Pediatr Rheumatol Online J 2017.