APA (7th ed.) Citation

Chen, W., Lin, Y., Xiong, Z., Wei, W., Ni, W., Tan, G., . . . Wu, Z. (2011). Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nature genetics, 43(12), 1252-1255. https://doi.org/10.1038/ng.1008

Chicago Style (17th ed.) Citation

Chen, Wan-Jin, et al. "Exome Sequencing Identifies Truncating Mutations in PRRT2 That Cause Paroxysmal Kinesigenic Dyskinesia." Nature Genetics 43, no. 12 (2011): 1252-1255. https://doi.org/10.1038/ng.1008.

MLA (9th ed.) Citation

Chen, Wan-Jin, et al. "Exome Sequencing Identifies Truncating Mutations in PRRT2 That Cause Paroxysmal Kinesigenic Dyskinesia." Nature Genetics, vol. 43, no. 12, 2011, pp. 1252-1255, https://doi.org/10.1038/ng.1008.