APA (7th ed.) Citation

Heussinger, N., Saake, M., Mennecke, A., Dörr, H., & Trollmann, R. (2017). Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity. Pediatric neurology, 67, 45-52. https://doi.org/10.1016/j.pediatrneurol.2016.10.007

Chicago Style (17th ed.) Citation

Heussinger, Nicole, Marc Saake, Angelika Mennecke, Helmuth-Günther Dörr, and Regina Trollmann. "Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity." Pediatric Neurology 67 (2017): 45-52. https://doi.org/10.1016/j.pediatrneurol.2016.10.007.

MLA (9th ed.) Citation

Heussinger, Nicole, et al. "Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity." Pediatric Neurology, vol. 67, 2017, pp. 45-52, https://doi.org/10.1016/j.pediatrneurol.2016.10.007.