Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis

MLA

Eber, Stefan W., et al. “Ankyrin–1 Mutations Are a Major Cause of Dominant and Recessive Hereditary Spherocytosis.” Nature Genetics, vol. 13, no. 2, June 1996, pp. 214–18. EBSCOhost, https://doi.org/10.1038/ng0696-214.

APA

Eber, S. W., Gonzalez, J. M., Lux, M. L., Scarpa, A. L., Tse, W. T., Dornwell, M., Herbers, J., Kugler, W., Ozcan, R., Pekrun, A., Gallagher, P. G., Schroter, W., Forget, B. G., & Lux, S. E. (1996). Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics, 13(2), 214–218. https://doi.org/10.1038/ng0696-214

Chicago

Eber, Stefan W., Jennifer M. Gonzalez, Marcia L. Lux, Alphonse L. Scarpa, William T. Tse, Marion Dornwell, Jutta Herbers, et al. 1996. “Ankyrin–1 Mutations Are a Major Cause of Dominant and Recessive Hereditary Spherocytosis.” Nature Genetics 13 (2): 214–18. doi:10.1038/ng0696-214.