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Numata, S; Koda, Y; Ihara, K; Sawada, T; Okano, Y; Matsuura, T; Endo, F; Yoo, HW; Arranz, JA; Rubio, V; Wermuth, B; Mew, NA; Tuchman, M; Pinner, JR; Kirk, EP; Yoshino, M (2010). Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations. Journal of human genetics, 55(1), pp. 18-22. Avenel, N.J.: Nature Publishing Group 10.1038/jhg.2009.113
Wallemacq, P; Maine, GT; Berg, K; Rosiere, T; Marquet, P; Aimo, G; Mengozzi, G; Young, J; Wonigeit, K; Kretschmer, R; Wermuth, B; Schmid, RW (2010). Multisite analytical evaluation of the Abbott ARCHITECT cyclosporine assay. Therapeutic drug monitoring, 32(2), pp. 145-151. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1097/FTD.0b013e3181d46386
Azevedo, L; Soares, P A; Quental, R; Vilarinho, L; Teles, E L; Martins, E; Diogo, L; Garcia, P; Cenni, B; Wermuth, B; Amorim, A (2006). Mutational spectrum and linkage disequilibrium patterns at the ornithine transcarbamylase gene (OTC). Annals of human genetics, 70(Pt 6), pp. 797-801. Oxford: Wiley-Blackwell 10.1111/j.1469-1809.2006.00283.x
