Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.

MLA

Mazereeuw-Hautier, J., et al. “Keratitis-Ichthyosis-Deafness Syndrome: Disease Expression and Spectrum of Connexin 26 (GJB2) Mutations in 14 Patients.” The British Journal of Dermatology, vol. 156, no. 5, May 2007, pp. 1015–19. EBSCOhost, https://doi.org/10.1111/j.1365-2133.2007.07806.x.

APA

Mazereeuw-Hautier, J., Bitoun, E., Chevrant-Breton, J., Man, S. Y. K., Bodemer, C., Prins, C., Antille, C., Saurat, J.-H., Atherton, D., Harper, J. I., Kelsell, D. P., & Hovnanian, A. (2007). Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients. The British Journal of Dermatology, 156(5), 1015–1019. https://doi.org/10.1111/j.1365-2133.2007.07806.x

Chicago

Mazereeuw-Hautier, J, E Bitoun, J Chevrant-Breton, S Y K Man, C Bodemer, C Prins, C Antille, et al. 2007. “Keratitis-Ichthyosis-Deafness Syndrome: Disease Expression and Spectrum of Connexin 26 (GJB2) Mutations in 14 Patients.” The British Journal of Dermatology 156 (5): 1015–19. doi:10.1111/j.1365-2133.2007.07806.x.