Unique patient with cerebrotendinous xanthomatosis. Evidence for presence of a defect in a gene that is not identical to sterol 27-hydroxylase.

MLA

Hansson, M., et al. “Unique Patient with Cerebrotendinous Xanthomatosis. Evidence for Presence of a Defect in a Gene That Is Not Identical to Sterol 27-Hydroxylase.” Journal of Internal Medicine, vol. 261, no. 5, May 2007, pp. 504–10. EBSCOhost, https://doi.org/10.1111/j.1365-2796.2007.01782.x.

APA

Hansson, M., Olin, M., Floren, C.-H., von Bahr, S., van’t Hooft, F., Meaney, S., Eggertsen, G., & Björkhem, I. (2007). Unique patient with cerebrotendinous xanthomatosis. Evidence for presence of a defect in a gene that is not identical to sterol 27-hydroxylase. Journal of Internal Medicine, 261(5), 504–510. https://doi.org/10.1111/j.1365-2796.2007.01782.x

Chicago

Hansson, M, M Olin, C-H Floren, S von Bahr, F van’t Hooft, S Meaney, G Eggertsen, and I Björkhem. 2007. “Unique Patient with Cerebrotendinous Xanthomatosis. Evidence for Presence of a Defect in a Gene That Is Not Identical to Sterol 27-Hydroxylase.” Journal of Internal Medicine 261 (5): 504–10. doi:10.1111/j.1365-2796.2007.01782.x.