1. Basistova, A.A., Langa, I.N., and Smirnova, G.V., Modern View of Lysosomal Diseases and Gaucher Disease, Pediatriya, 1999, no. 4, pp. 90–93.
2. Germain, D.P., Gaucher’s Disease. A Paradigm for Interventional Genetics, Clin. Genet., 2004, vol. 65, no. 2, pp. 77–86.
3. Beutler, E. and Grabowski, G.A., Gaucher Disease, in The Metabolic and Molecular Bases of Inherited Disease, Scriver, C.R., Beaudet, A.L., Sly, W.S., and Valle, D., Eds., New York: McGraw-Hill, 2001, pp. 3635–3668.
4. Horowitz, M., Wildre, S., Horowitz, Z., Reiner, O., Gelbart, T., and Beutler, E., The Human Glucocerebrosidase Gene and Pseudogene: Structure and Evolution, Genomics, 1989, vol. 4, no. 1, pp. 87–96.
5. Montfort, M., Chabas, A., Vilageliu, L., and Grinberg, D., Functional Analysis of 13 GBA Mutant Alleles Identified in Gaucher Disease Patients: Pathogenic Changes and “Modifier” Polymorphisms, Human Mutat., 2004, vol. 23, pp. 567–575.