Author:
Ben-Yoseph Y.,Baylerian M. S.,Momoi T.,Nadler H. L.
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Beutler, E. The biochemical genetics of the hexosaminidase system in man.Am. J. Hum. Genet. 31 (1979) 95–105
2. Beutler, E., Villacorte, D., Kuhl, W., Guinto, E. and Srivastava, S. Nonenzymatic conversion of human hexosaminidase A.J. Lab. Clin. Med. 86 (1975a) 195–203
3. Beutler, E., Kuhl, W. and Comings, D. Hexosaminidase isozyme in type 0 GM2 gangliosidosis (Sandhoff-Jatzkewitz disease).Am. J. Hum. Genet. 27 (1975b) 628–638
4. Bradford, M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.Anal. Biochem. 72 (1976) 248–254
5. Conzelmann, E. and Sandhoff, K. AB Variant of infantile GM2 gangliosidosis: Deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.Proc. Natl. Acad. Sci. USA 75 (1978) 3979–3983
Cited by
7 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