1. Ahern-Rindell, A. J., Stone, D. M., Parish, S. M., Leathers, C. W., and Prieur, D. J. (1985). A neuronal lysosomal storage disease in sheep associated with a deficiency of β-galactosidase.Fed. Proc. Abstr. 44744.
2. Ahern-Rindell, A. J., Prieur, D. J., and Murnane, R. D. (1986). An inherited lysosomal storage disease of sheep associated with deficiencies of β-galactosidase and α-neuraminidase.Am. J. Hum. Genet. Abstr. 39:A3.
3. Ahern-Rindell, A. J., Murnane, R. D., and Prieur, D. J. (1988a). Deficiency of β-galactosidase activity in tissues of sheep affected with a lysosomal storage disease.FASEB J. Abstr. 2:A397.
4. Ahern-Rindell, A. J., Prieur, D. J., Murnane, R. D., Raghavan, S. S., Daniel, P. F. McCluer, R. H., Walkley, S. U., and Parish, S. M. (1988b). Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep.Am. J. Med. Genet. 3139.
5. Ben-Yoseph, Y., Shapira, E., Edelman, D., Burton, B., and Nadler, H. L. (1977). Purification and properties of neutral β-galactosidase from human liver.Arch. Biochem. Biophys. 184373.