Saillour, Y., Zanni, G., Des Portes, V., Heron, D., Guibaud, L., Iba-Zizen, M. T., . . . Bienvenu, T. (2007). Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia. Journal of medical genetics, 44(11), 739-744. https://doi.org/10.1136/jmg.2007.051334
Chicago Style (17th ed.) CitationSaillour, Y., et al. "Mutations in the AP1S2 Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex Are Associated with Syndromic X-linked Mental Retardation with Hydrocephalus and Calcifications in Basal Ganglia." Journal of Medical Genetics 44, no. 11 (2007): 739-744. https://doi.org/10.1136/jmg.2007.051334.
MLA (9th ed.) CitationSaillour, Y., et al. "Mutations in the AP1S2 Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex Are Associated with Syndromic X-linked Mental Retardation with Hydrocephalus and Calcifications in Basal Ganglia." Journal of Medical Genetics, vol. 44, no. 11, 2007, pp. 739-744, https://doi.org/10.1136/jmg.2007.051334.