Author:
Reuser A. J. J.,Willemsen R.,van der Ploeg A. T.,Kroos M.,Hoefsloot E. H.,Oostra B. A.
Reference49 articles.
1. J.B. Stanbury, J.B. Wyngaarden, D.S. Fredrickson, J.L. Goldstein and M.S. Brown, eds., The Metabolic Basis of Inherited Disease, 5th ed., McGraw-Hill, New York (1983).
2. H.G. Hers and F. Van Hoof, eds., Lysosomes and Storage Diseases, Academic Press, New York (1973).
3. V.A. McKusick, Phenotypic diversity of human diseases resulting from allelic series, Am. J. Hum. Genet. 25:446 (1973).
4. S. Okada, and J.S. O’Brien, Tay-Sachs disease: Generalized absence of a 3-D-N-acetylhexosaminidase component, Science 165:698 (1969).
5. K. Sandhoff, U. Andrea, and H. Jatzkewitz, Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs, Life Sci. 7:283 (1968).
Cited by
1 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