Reed, K., Tucker, D. E., Aloulou, A., Adler, D., Ghomashchi, F., Gelb, M. H., . . . Boutaud, O. (2011). Functional characterization of mutations in inherited human cPLA(2) deficiency.

Reed, Kathleen, Dawn E. Tucker, Ahmed Aloulou, David Adler, Farideh Ghomashchi, Michael H. Gelb, Christina C. Leslie, John A. Oates, and Olivier Boutaud. Functional Characterization of Mutations in Inherited Human CPLA(2) Deficiency. 2011.

Reed, Kathleen, et al. Functional Characterization of Mutations in Inherited Human CPLA(2) Deficiency. 2011.