1. Aisen, P., Shorr, J. B., Morell, A. G., Gold, P. Z., Scheinberg, I. H.: A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson’s disease. Amer. J. Med. 28, 550–554 (1960).
2. André, M. J., van Bogaert, L.: L’hérédité dans dégénérescence hepato-lenticulaire et le probleme des rapports intrinseques de la pseudosclérose de Westphal-Strümpell et de la maladie de Wilson. Encéphale 39, 1–54 (1950).
3. Arima, M., Kurumada, T.: Genetical studies of Wilson’s disease in children. II. Mode of inheritance and gene frequency in Japan. Pediat. Univ. Tokyo 5, 14–19 (1962).
4. Aspin, N., Sass-Kortsak, A.: Radiocopper studies on a family with Wilson’s disease. In: The biochemistry of Copper (J. Peisach, P. Aisen, and W. E. Blumberg, Eds.), pp. 503–512. New York: Academic Press 1966.
5. Barbeau, A., Friesen, H.: Treatment of Wilson’s disease with L-dopa after failure with Penicillamine. Lancet 1970 I, 1180–1181.