Glycoprotein Storage Diseases and the Mucopolysaccharidoses
Reference131 articles.
1. Akasaki, M., Sugahara, K., Funakoshi, I., Aula, P., and Yamashina, I., 1976, Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartyl- glycosaminuria, FEBS Lett. 69: 91. 2. Alhadeff, J. A., Miller, A. L., Wenaas, H., Vedvick, T., and O’Brien, J. S., 1975, Human liver a-L-fucosidase: Purification, characterization and immunochemical studies, J. Biol. Chem. 250: 7106. 3. Arbisser, A. I., Donnelly, K. A., Scott, C. I., Jr., DiFerrante, N., Singh, J., Stevenson, R. E., Aylesworth, A. S., and Howell, R. R., 1978, Morquio-like syndrome with 0-galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IV B, Am. J. Med. Genet. 1: 195. 4. Austin, J. H., 1973, Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency, Arch. Neurol. 28: 258. 5. Autio, S., 1972, Aspartylglucosaminuria: Analysis of thirty-four patients, J. Ment. Defic. Res. Monogr. Ser. 1: 1.
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|