APA (7th ed.) Citation

Klein, C., Grudzien, M., Appaswamy, G., Germeshausen, M., Sandrock, I., Schäffer, A. A., . . . Welte, K. (2007). HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nature Genetics, 39(1), 86. https://doi.org/10.1038/ng1940

Chicago Style (17th ed.) Citation

Klein, Christoph, et al. "HAX1 Deficiency Causes Autosomal Recessive Severe Congenital Neutropenia (Kostmann Disease)." Nature Genetics 39, no. 1 (2007): 86. https://doi.org/10.1038/ng1940.

MLA (9th ed.) Citation

Klein, Christoph, et al. "HAX1 Deficiency Causes Autosomal Recessive Severe Congenital Neutropenia (Kostmann Disease)." Nature Genetics, vol. 39, no. 1, 2007, p. 86, https://doi.org/10.1038/ng1940.