APA (7th ed.) Citation

Vannier, C., Behnisch, W., Bartsch, I., Sandrock, K., Ertle, F., Schmidt, K., . . . Zieger, B. (2010). Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I. Klinische Pädiatrie, 222(3), . https://doi.org/10.1055/s-0030-1249064

Chicago Style (17th ed.) Citation

Vannier, Corinne, et al. "Novel Homozygous Mutation (c.175delG) in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann's Thrombasthenia Type I." Klinische Pädiatrie 222, no. 3 (2010). https://doi.org/10.1055/s-0030-1249064.

MLA (9th ed.) Citation

Vannier, Corinne, et al. "Novel Homozygous Mutation (c.175delG) in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann's Thrombasthenia Type I." Klinische Pädiatrie, vol. 222, no. 3, 2010, https://doi.org/10.1055/s-0030-1249064.