Cite
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.
MLA
Huckert, Mathilde, et al. “Mutations in the Latent TGF-Beta Binding Protein 3 (LTBP3) Gene Cause Brachyolmia with Amelogenesis Imperfecta.” Human Molecular Genetics, vol. 24, no. 11, June 2015, pp. 3038–49. EBSCOhost, https://doi.org/10.1093/hmg/ddv053.
APA
Huckert, M., Stoetzel, C., Morkmued, S., Laugel-Haushalter, V., Geoffroy, V., Muller, J., Clauss, F., Prasad, M. K., Obry, F., Raymond, J. L., Switala, M., Alembik, Y., Soskin, S., Mathieu, E., Hemmerlé, J., Weickert, J.-L., Dabovic, B. B., Rifkin, D. B., Dheedene, A., … Bloch-Zupan, A. (2015). Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. Human Molecular Genetics, 24(11), 3038–3049. https://doi.org/10.1093/hmg/ddv053
Chicago
Huckert, Mathilde, Corinne Stoetzel, Supawich Morkmued, Virginie Laugel-Haushalter, Véronique Geoffroy, Jean Muller, François Clauss, et al. 2015. “Mutations in the Latent TGF-Beta Binding Protein 3 (LTBP3) Gene Cause Brachyolmia with Amelogenesis Imperfecta.” Human Molecular Genetics 24 (11): 3038–49. doi:10.1093/hmg/ddv053.