Jacquot, S., Merienne, K., De Cesare, D., Pannetier, S., Mandel, J. L., Sassone-Corsi, P., & Hanauer, A. (1998). Mutation analysis of the RSK2 gene in Coffin-Lowry patients: Extensive allelic heterogeneity and a high rate of de novo mutations.

Jacquot, S., K. Merienne, D. De Cesare, S. Pannetier, J L. Mandel, P. Sassone-Corsi, a A. Hanauer. Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations. 1998.

Jacquot, S., et al. Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations. 1998.