The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.

MLA

Nakashima, Mitsuko, et al. “The Somatic GNAQ Mutation c.548G>A (p.R183Q) Is Consistently Found in Sturge-Weber Syndrome.” Journal of Human Genetics, vol. 59, no. 12, Dec. 2014, pp. 691–93. EBSCOhost, https://doi.org/10.1038/jhg.2014.95.

APA

Nakashima, M., Miyajima, M., Sugano, H., Iimura, Y., Kato, M., Tsurusaki, Y., Miyake, N., Saitsu, H., Arai, H., & Matsumoto, N. (2014). The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome. Journal of Human Genetics, 59(12), 691–693. https://doi.org/10.1038/jhg.2014.95

Chicago

Nakashima, Mitsuko, Masakazu Miyajima, Hidenori Sugano, Yasushi Iimura, Mitsuhiro Kato, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Hajime Arai, and Naomichi Matsumoto. 2014. “The Somatic GNAQ Mutation c.548G>A (p.R183Q) Is Consistently Found in Sturge-Weber Syndrome.” Journal of Human Genetics 59 (12): 691–93. doi:10.1038/jhg.2014.95.