Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.

MLA

Hassan, H., et al. “Severe Meesmann’s Epithelial Corneal Dystrophy Phenotype Due to a Missense Mutation in the Helix-Initiation Motif of Keratin 12.” Eye (London, England), vol. 27, no. 3, Mar. 2013, pp. 367–73. EBSCOhost, https://doi.org/10.1038/eye.2012.261.

APA

Hassan, H., Thaung, C., Ebenezer, N. D., Larkin, G., Hardcastle, A. J., & Tuft, S. J. (2013). Severe Meesmann’s epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12. Eye (London, England), 27(3), 367–373. https://doi.org/10.1038/eye.2012.261

Chicago

Hassan, H, C Thaung, N D Ebenezer, G Larkin, A J Hardcastle, and S J Tuft. 2013. “Severe Meesmann’s Epithelial Corneal Dystrophy Phenotype Due to a Missense Mutation in the Helix-Initiation Motif of Keratin 12.” Eye (London, England) 27 (3): 367–73. doi:10.1038/eye.2012.261.