Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

MLA

Strømme, Petter, et al. “Mutations in the Human Ortholog of Aristaless Cause X-Linked Mental Retardation and Epilepsy.” Nature Genetics, vol. 30, no. 4, Apr. 2002, pp. 441–45. EBSCOhost, https://doi.org/10.1038/ng862.

APA

Strømme, P., Mangelsdorf, M. E., Shaw, M. A., Lower, K. M., Lewis, S. M. E., Bruyere, H., Lütcherath, V., Gedeon, A. K., Wallace, R. H., Scheffer, I. E., Turner, G., Partington, M., Frints, S. G. M., Fryns, J.-P., Sutherland, G. R., Mulley, J. C., & Gécz, J. (2002). Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy. Nature Genetics, 30(4), 441–445. https://doi.org/10.1038/ng862

Chicago

Strømme, Petter, Marie E Mangelsdorf, Marie A Shaw, Karen M Lower, Suzanne M E Lewis, Helene Bruyere, Viggo Lütcherath, et al. 2002. “Mutations in the Human Ortholog of Aristaless Cause X-Linked Mental Retardation and Epilepsy.” Nature Genetics 30 (4): 441–45. doi:10.1038/ng862.