Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

MLA

Southgate, Laura, et al. “Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies.” American Journal of Human Genetics, vol. 88, no. 5, May 2011, pp. 574–85. EBSCOhost, https://doi.org/10.1016/j.ajhg.2011.04.013.

APA

Southgate, L., Machado, R. D., Snape, K. M., Primeau, M., Dafou, D., Ruddy, D. M., Branney, P. A., Fisher, M., Lee, G. J., Simpson, M. A., He, Y., Bradshaw, T. Y., Blaumeiser, B., Winship, W. S., Reardon, W., Maher, E. R., FitzPatrick, D. R., Wuyts, W., Zenker, M., … Trembath, R. C. (2011). Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. American Journal of Human Genetics, 88(5), 574–585. https://doi.org/10.1016/j.ajhg.2011.04.013

Chicago

Southgate, Laura, Rajiv D Machado, Katie M Snape, Martin Primeau, Dimitra Dafou, Deborah M Ruddy, Peter A Branney, et al. 2011. “Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies.” American Journal of Human Genetics 88 (5): 574–85. doi:10.1016/j.ajhg.2011.04.013.