de Vooght, K. M., van Solinge, W. W., van Wesel, A. C., Kersting, S., & van Wijk, R. (2009). First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis. Ferrata Storti Foundation.

de Vooght, Karen M.K., Wouter W. van Solinge, Annet C. van Wesel, Sabina Kersting, und Richard van Wijk. First Mutation in the Red Blood Cell-specific Promoter of Hexokinase Combined With a Novel Missense Mutation Causes Hexokinase Deficiency and Mild Chronic Hemolysis. Ferrata Storti Foundation, 2009.

de Vooght, Karen M.K., et al. First Mutation in the Red Blood Cell-specific Promoter of Hexokinase Combined With a Novel Missense Mutation Causes Hexokinase Deficiency and Mild Chronic Hemolysis. Ferrata Storti Foundation, 2009.