Mouton, J. M., Kinnear, C. J., Moolman-Smook, J. C., Herbst, P. G., Pellizzon, A. S., Goosen, A., & Brink, P. A. (2015). Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy. Cardiovasc J Afr.

Mouton, Jomien M., Craig J. Kinnear, Johanna C. Moolman-Smook, Philip G. Herbst, Adriano S. Pellizzon, Althea Goosen, und Paul A. Brink. "Diagnostic Disparity and Identification of Two TNNI3 Gene Mutations, One Novel and One Arising De Novo, in South African Patients With Restrictive Cardiomyopathy and Focal Ventricular Hypertrophy." Cardiovasc J Afr 2015.

Mouton, Jomien M., et al. "Diagnostic Disparity and Identification of Two TNNI3 Gene Mutations, One Novel and One Arising De Novo, in South African Patients With Restrictive Cardiomyopathy and Focal Ventricular Hypertrophy." Cardiovasc J Afr 2015.