APA (7th ed.) Citation

Rauch, A., Rappold, G., & Wieacker, P. (2012). Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: An exome sequencing study. The lancet, 380(9854), . https://doi.org/10.1016/S0140-6736(12)61480-9

Chicago Style (17th ed.) Citation

Rauch, Anita, Gudrun Rappold, and Peter Wieacker. "Range of Genetic Mutations Associated with Severe Non-syndromic Sporadic Intellectual Disability: An Exome Sequencing Study." The Lancet 380, no. 9854 (2012). https://doi.org/10.1016/S0140-6736(12)61480-9.

MLA (9th ed.) Citation

Rauch, Anita, et al. "Range of Genetic Mutations Associated with Severe Non-syndromic Sporadic Intellectual Disability: An Exome Sequencing Study." The Lancet, vol. 380, no. 9854, 2012, https://doi.org/10.1016/S0140-6736(12)61480-9.