Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis - Gandrille, S; Vidaud, M; Aiach, M; Alhenc-Gelas, M; Fisher, A M; Gouault-Heilman, M; Toulon, P; Fiessinger, J N; Goossens, M (Human Mutation, 1992)