Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Beutler E., Kuhl W. Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae. Am J Hum Genet. 1972 May;24(3):237–249. [PMC free article] [PubMed] [Google Scholar]
- Beutler E., Kuhl W. Fabry's disease: structural or regulatory mutation? J Lab Clin Med. 1971 Dec;78(6):987–987. [PubMed] [Google Scholar]
- Beutler E., Kuhl W. Purification and properties of human alpha-galactosidases. J Biol Chem. 1972 Nov 25;247(22):7195–7200. [PubMed] [Google Scholar]
- Goldstone A., Konecny P., Koenig H. Lysosomal hydrolases: Conversion of acidic to basic forms by neuraminidase. FEBS Lett. 1971 Feb 12;13(1):68–72. doi: 10.1016/0014-5793(71)80667-1. [DOI] [PubMed] [Google Scholar]
- Ho M. W., Beutler S., Tennant L., O'Brien J. S. Fabry's disease: evidence for a physically altered -galactosidase. Am J Hum Genet. 1972 May;24(3):256–266. [PMC free article] [PubMed] [Google Scholar]
- Kint J. A. Fabry's disease: alpha-galactosidase deficiency. Science. 1970 Feb 27;167(3922):1268–1269. doi: 10.1126/science.167.3922.1268. [DOI] [PubMed] [Google Scholar]
- Kint J. A. On the existence and the enzymic interconversion of the isozymes of alpha-galactosidase in human organs. Arch Int Physiol Biochim. 1971 Aug;79(3):633–634. [PubMed] [Google Scholar]