Southgate, L., Machado, R., Snape, K., Primeau, M., Dafou, D., Ruddy, D., . . . Trembath, R. (2011). Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies. Elsevier.
Chicago Style CitationSouthgate, Laura, et al. Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies. Elsevier, 2011.
Cita MLASouthgate, Laura, et al. Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies. Elsevier, 2011.
Atenció: Aquestes cites poden no estar 100% correctes.